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октября 10, 2019

Drugs & drug paraphernalia



This page covers drugs, controlled substances, and drug paraphernalia. A drug is a substance used to diagnose, cure, treat, or prevent diseases in people or animals. Drugs can also be used to change the structure or function of the body, such as to treat some kinds of acne. Some drugs require a prescription for sale, such as most antibiotics, while other drugs may be sold without a prescription because they are approved by the FDA to be sold over the counter.



“Controlled substances” are drugs that are illegal, such as cocaine or heroin. Products used with controlled substances may be considered drug paraphernalia. Drug paraphernalia includes products primarily intended or designed for use in making, preparing, or using a controlled substance.



Please use the checklist below to be sure your product can be sold on Amazon.



Compliance Checklist for Drugs & Drug Paraphernalia



Packaging

Drugs must be sealed in the original manufacturer’s packaging Drugs must be new and unused Drugs must clearly display identifying codes placed on the packaging by the manufacturer or distributor, such as matrix codes, lot numbers, or serial numbers



Labeling

Drugs must be labeled in English with the following information:

The title of the drug The “Drug Facts” panel The active ingredient(s) The purpose(s) of the drug The use(s) of the drug Any required warning(s) The directions for using the drug Any other information, as required for the specific product The inactive ingredients Drug must use the claim “FDA approved” appropriately Drug labels must not use the FDA logo



For more information, see the U. S. Food and Drug Administration’s Guidance on Labeling and Is It Really 'FDA Approved?'



Detail page

Detail pages must include the following information:

The name of the drug The active ingredients An image of the “Drug Facts” panel (and any “Drug Facts (Continued)” panels, if applicable) from the product label Detail pages must comply with the approved labeling for the drug Drug must use the claim “FDA approved” appropriately Drug labels must not use the FDA logo



Drug products and ingredients

Drug products must be approved by the FDA for over-the-counter (OTC) sale Drug products must not require a prescription or a medical professional's supervision or direction for their use, such as:

Prescription drugs and their active ingredients Antibiotics (including "fish" antibiotics, both over-the-counter and prescription) Prescription veterinary products and their active ingredients Vaccines (including human and animal vaccines) Drug products must not be named in an FDA recall or safety alert (for more information, see: Recalls, Market Withdrawals, & Safety Alerts) Drug products must not have been the subject of a Drug Enforcement Administration (DEA) emergency scheduling (for more information, see: DEA Press Releases) Drug products must not be named by the Federal Trade Commission (FTC) as making untrue marketing claims (for more information, see: Federal Trade Commission Press Releases) Drug products must not be identified as adulterated (e. g. unsafe or lacking evidence of safety) or misbranded (e. g. having false or misleading information on the label) in an FDA warning letter (for more information, see: FDA Warning Letters) Drug listings must not be for controlled substances or products containing controlled substances, such as:

Hemp products containing Resin or tetrahydrocannabinol (THC) Hemp (or any cannabis Sativa spp. strain) seeds capable of germination Anything listed in Schedules I, II, III, IV or V of the Controlled Substances Act (for more information, see: Schedules of Controlled Substances), such as:

Coca Leaves, including all variations of leaves, tea, and coca extract Hallucinogenic mushrooms Poppy pods, poppy straw, and poppy straw concentrate "List I" chemicals or their derivatives as designated by the Drug Enforcement Administration (DEA) (for more information, see: List I and List II Chemicals), such as:

Ephedrine Phenylpropanalomine Pseudoephedrine Ergotamine



Known prohibited products



Amazon specifically prohibits the following drug products, controlled substances, and products imitating drug products and controlled substances. These products are prohibited because they do not meet the checklist requirements. This list does not include all drug products prohibited by Amazon.




    Amanita muscaria Clenbuterol Coca Leaves, including all variations of leaves, tea, and coca extract Codeine Damiana Dimethyltryptamine (DMT) Drotebanol Ephedrine Ergotamine Hawaiian Baby Woodrose or Argyreia Nervosa seeds Jimson Weed Kanna Ketamine Ketamine Klip Dagga Kratom Marshmallow Leaf Panther amanitas Peyote or mescaline Phenylpropanalomine Poppers, amyl nitrite products, or related products Poppy pods, poppy straw, and poppy straw concentrate Poppy tea (tea brewed from poppy seeds, pods, or straw) Pseudoephedrine Psilocybe Cubensis Psilocybin Salvia Divinorum Sonoran Song Mimosa Hostilis Syrian Rue Wild Dagga Yopo Seeds



Amazon. com Help: Safety Information, Recalls, Warranties & Legal Notices



Dear Specialized Rider,



We committed to keeping you updated on the progress of the impending recall of Öhlins RXF Air Forks as originally communicated on September 17, 2018.



We’re happy to update that Öhlins has been making progress with this investigation and has submitted a technical report to the appropriate government agencies for review. There are many factors affecting the timeline to full approval, so we can't project a date. Our Quality, Legal, and Rider Care teams, however, are directly engaged with both Öhlins and the regulatory agencies to help expedite the process.



We realize that you bought your bike expecting to actually ride it, and this issue is disrupting your trips, races, and rides with friends. As we work with Öhlins towards a safe and compliant permanent fix, we're committed to using all of our resources to keep you riding. We have a limited quantity of loaner forks that we can provide to your retailer for temporary use. Availability varies by region, but we encourage you to contact your retailer and we'll work with them to support you.



We will continue to provide weekly progress updates on this page, so please check back with us here next week.



Thanks again for your patience and thanks for riding Specialized.



Director, Global Quality and Rider Care



September 17, 2018: Ohlins RXF



Dear Specialized Rider,



At Specialized, your safety is our primary concern. So, whenever this is compromised, we take immediate action.



Based upon reports from the field, we've concluded that the Öhlins RXF 36 29/27.5+ and 27.5” Air Forks that are spec’d as original equipment on the 2017 Stumpjumper, Enduro, and Fuse, the 2018 Stumpjumper, Enduro, Turbo Levo, and Fuse, and the Öhlins RXF 34 Air fork sold separately in the aftermarket, may contain a defect in the top cap which potentially affects safety. Specifically, the right-side top cap on some forks may not be adequately torqued, which in some cases, may lead to the top cap working itself free through riding. When this happens, the air cartridge may abruptly spring out of the stanchion tube causing a risk of injury to the rider. Therefore, we've decided to ask riders to stop riding, and our retailers to stop selling, affected forks and bicycles.



We are working, urgently, in partnership with Öhlins on a remedy to this issue. Once we have obtained the necessary government approvals on our solution, we will issue a recall to fix the forks and get you back riding. As we progress with our recall strategy and approvals, we will provide weekly updates on this page.



Please note that other Öhlins Forks, such as the RXF 36 Coil forks, are unaffected by this notice.



We wish to apologize for this inconvenience and thank you for your patience.



Thanks for riding Specialized.



Director, Global Quality and Rider Care



Update 2/15/2018: Allez



Thank you for your patience as we've worked to address the safety concern relating to Model Year 2018 Allez (Base), Allez Sport, and Allez Elite forks.



We're happy to report that we've received approval for our fork recall and replacement program, and we've been working hard to source replacement forks to get you back riding as quickly as possible. Starting today, we will begin delivery of forks to your retailer, who will install the new fork on your bike at no cost to you.



As we've stated before, availability of forks will initially be limited, but we expect more forks to arrive each week. We anticipate having sufficient quantities to serve all riders globally by the end of March at the latest.



Your retailer will be contacting you via email to provide further detail on the recall and the replacement program. When a fork is available to match your bike, your retailer will contact you to schedule the replacement at your convenience.



Please email [email protected] or call directly at (800) 722-4423 if you have any questions.



On behalf of the Global Rider Care team, thank you for riding Specialized.



Director, Global Quality and Rider Care



Dear Specialized Rider:



At Specialized, it's our priority to ensure that you, our rider, can use our products safely and with confidence.



We have identified a very small number of Stout cranks with direct-mount chainrings (sold only with our MY18 Fuse Comp and Fatboy SE models) that may have been manufactured with an important dimension out of tolerance. In extreme, and very rare cases, this production variation could lead to the drive-side crankarm disengaging from the crank assembly, causing a risk of injury. Only cranks manufactured in 2017 are potentially affected.



By this letter, we are announcing a voluntary recall of affected cranks, which have a serial code beginning with “17” embossed on the inside of either crankarm. We have partnered with the crank manufacturer to improve the manufacturing process, as well as to provide you with a like-for-like replacement of your crankarm. These replacement parts are available immediately and may be obtained by contacting your Authorized Specialized Retailer. Your retailer may also reach out to you directly. In any case, you should stop riding your affected bike until the replacement crank has been installed.



To obtain your replacement crankarm, contact your retailer. Your retailer will help you identify whether your bike is affected and will obtain the replacement parts from Specialized. In most cases, we will have you back riding within 48 hours of retailer contact.



For questions, please contact Specialized Rider Care at (877) 808-8154



Thanks for your understanding, and we sincerely apologize for the trouble.



Director, Global Quality and Rider Care



In December we issued a notice asking you to stop riding your affected Allez, and that we'd replace your fork with a new one painted to match. At this time, we are happy to update that production of replacement forks is going according to plan and without delay. Pending regulatory approval, we expect being able to replace forks beginning in early February.



Please be aware that while our team is working hard with our suppliers to meet global demand, initial quantities will be limited. We will be allocating forks on a first-come, first-served basis. Priority will be given to riders who have signed up in advance at their retailer. If you have not done so already, we invite you to contact your retailer and provide your bike details and contact information so that we can prioritize your replacement.



When you sign up for a new fork, we will offer you a credit of $75 to use on Specialized merchandise at your local retailer. Please note this pre-order is NOT necessary to be eligible for a new fork or the $75 gift from Specialized, but it will help us get you a fork as quickly as possible.



Our next communication on this topic will be in early February. At that time we should be able to provide specific details to you and your retailer to get you a new fork. In the meantime, if you have any questions, please contact your retailer or Specialized Rider Care.



Thanks again for your patience, and thanks for riding Specialized.



Jon Goulet, Director of Global Quality and Rider Care



Thank you for being a Specialized customer. We have been working on a safety improvement that needs to be made to your current Venge ViAS. Specialized has received isolated reports from the field of the rear wheel coming out of the rear dropouts, which can cause fractures in the rear triangle. Please read Specialized’s notice below.



Your safety is of the upmost importance to Specialized and your retailer partner At this time please stop riding your Venge ViAS Rim. We ask that you bring your bike to our shop so we can install the replacement rear derailleur hanger. This will be of no cost to you.



Please email [email protected] or call directly at (800)722-4423 if you have any questions. We appreciate your cooperation with this update.



Dear Specialized Rider:



At Specialized, safety is our primary concern, and when safety is compromised for the rider, we need to take action.



After careful examination, we've concluded that some model year 2018 Allez, Allez Elite, and Allez Sport model bikes may contain a manufacturing defect in the fork crown which potentially affects safety. Therefore, we've decided to prepare for a recall which will involve replacing the existing fork with a new fork.



By this letter, we're asking riders to stop riding, and our dealers to stop selling, affected bicycles. Even though, to our knowledge, no one has been injured and no regulatory agency has brought this to our attention.



We've already engaged our considerable manufacturing resources to supply high-quality replacement forks, painted to match your bikes. Riders who've purchased these bikes will be our first priority for replacement, followed by our retailers. As riders ourselves, we fully understand and are working hard at finding solutions to minimize your inconvenience. We hope you'll understand and appreciate that we will need time to obtain necessary government approvals and time for our factories to produce a sufficient quantity of forks for the recall.



We assure you that getting you, the rider, back on your bike is our highest priority, and that we're working day and night to make this happen as quickly as possible. As we progress, we'll provide regular updates to you on Specialized. com. And when we begin to deliver replacement forks, we will promptly notify all concerned.



For questions, please contact Specialized Rider Care at (877) 808-8154.



On our part, we wish to apologize for this inconvenience.



Mark Schroeder, Director of Engineering



By submitting your email address you agree to the Terms & Conditions



Hornet 22 Product Safety Warning And Recall Notice



Safety Warning And Recall Notice



Product Safety Recall Notice



Warning - Do Not Use



REMINGTON 22 HORNET 45 GR PSP AMMUNITION WITH LOT NOS. J29EAI, J29EBI, J30EAI, J30EBI OR K01JDI



Remington has determined that five Lots of its 22 Hornet 45 Gr PSP ammunition may have improper powder charge weights. The five Lot Numbers are identified above. Improper powder charge weights may result in a malfunction of the cartridge when the firearm is fired. This malfunction may result in a bullet being lodged in the barrel creating an obstruction. If another round is fired with an obstruction in the barrel, a barrel burst may occur. A barrel burst could result in property damage, serious personal injury or death.



Do Not Use



Remington 22 Hornet 45 Gr PSP Ammunition Lot Numbers J29EAI, J29EBI, J30EAI, J30EBI OR K01JDI



To identify if you have one of these Lots of ammunition:




    If you have a case of 22 Hornet 45 Gr PSP ammunition the Lot Number is stenciled on the outside of the case; and, If you have a box of 22 Hornet 45 Gr PSP ammunition the Lot Number is stamped on the inside flap of the box.



If you have any of this Remington 22 Hornet 45 Gr PSP ammunition, as identified above, immediately discontinue use of this ammunition and contact Remington at the below telephone number. Remington will arrange for the return shipment of your ammunition and upon receipt will send you replacement ammunition at no cost to you. If you are unsure whether or not you have one or more of these Lots of ammunition or if you have mixed boxes of ammunition; please immediately discontinue the use of the ammunition and contact Remington at the below telephone number – we will replace this ammunition for you.



For any consumer questions or instructions on how to return of your Remington 22 Hornet 45 Gr PSP ammunition with one of the following Lot Numbers J29EAI, J29EBI, J30EAI, J30EBI OR K01JDI, please contact the Remington Consumer Service Department at 1-800-243-9700, Prompt #4.



The only Remington 22 Hornet 45 Gr PSP ammunition affected by this recall has one of the following Lot Numbers J29EAI, J29EBI, J30EAI, J30EBI OR K01JDI. No other Lots or ammunition is affected.



We apologize for any inconvenience this may cause.



Safety First



Always observe the Ten Commandments of Firearm Safety and wear approved eye and ear protection anytime you are shooting.



Port Ludlow Fire & Rescue - plfr. org



Fire Chief Brad Martin



Headquarters

Station No. 31



7650 Oak Bay Road

Port Ludlow, WA 98365



Business Hours:

8am-4:30pm, Mon-Fri



1-360-437-2236 phone

1-360-437-9184 fax

1-866-367-2291 fax *



* confidential for HIPAA, medical records, etc.







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General Safety Notices and Product Recalls




November 2017

Kidde Fire Extinguishers with Plastic Handles Recalled



KIDDE brand Fire Extinguishers with plastic handles have been recalled. Please forward this information to anyone you may know. This is a major recall, so pay close attention to the details in the following link.



Port Ludlow Fire & Rescue does not accept any used/old/recalled Fire Extinguishers. As your Fire Chief, I am passing this information along as a safety issue to all community members.



There is a toll free number to call KIDDE for directions on how to replace your extinguisher should you find you have a recalled unit. The number is 855-271-0773.



June 9, 2016

State Fire Marshals Urge Amazon and Other Retailers to Remove Potentially Unsafe Fire Safety Products



The National Association of State Fire Marshals (NASFM), an association whose principal membership comprises the senior fire officials in the United States and their top deputies, is asking the country's largest online retailer to stop the sale of smoke alarms that are not tested to nationally-recognized standards and which may not comply with applicable building codes in many states and municipalities. В NASFM is also asking the Consumer Product Safety Commission (CPSC) to take action to ensure consumers are protected and purchasing safe products.



In question are smoke alarms that do not carry the testing labels from a Nationally Recognized Third Party Testing Laboratory such as Underwriter Laboratories (UL) or Intertek/ETL – the two largest independent safety testing companies for electrical products.  Products with these marks are evidence that the smoke alarm has been independently tested and complies with UL 217, Standard for Smoke Alarms, the industry-accepted standard for smoke alarms.



NASFM identified several smoke alarm brands lacking third party testing laboratory marks on Amazon including: X-Sense, Arikon and Bovon.



Browning explained that smoke alarms sold in the United States are sent to UL or Intertek/ETL for testing and review. The two testing companies test smoke alarms in accordance to the UL 217 standard, the industry-accepted standard. В Products not tested to this standard may not accurately detect fire, alarm the consumer in a timely fashion, and operate for the desired time period or other critical functions. В Browning noted that the third-party listing also protects the consumer from potential legal penalties. В В



About NASFM, "50 States – One Strong Voice for Fire Prevention"

The principal membership of NASFM comprises the senior fire officials in the United States and their top deputies. The primary mission of the National Association of State Fire Marshals (NASFM) is to protect human life, property and the environment from fire and related hazards.



Learn more about NASFM and its issues at www. firemarshals. org



September 18, 2014

Kidde AC/DC smoke alarm and combination smoke/carbon monoxide alarm recall





Walter Kidde Portable Equipment Inc. ("Kidde") in conjunction with the U. S. Consumer Product Safety Commission (CPSC) announced a voluntary recall to replace certain Kidde AC/DC smoke alarms and combination smoke/carbon monoxide alarms. A copy of the joint recall announcement can be seen by clicking here and attached is the safety notice. Kidde has sent copies to our retail customers with instructions to post a copy of the safety notice in stores that sold these alarms.



This replacement program was initiated because the units may not perform as designed following a power outage. If a power outage occurs at the same second that a unit is performing a sensor health check, the units may go into a "latched" mode, causing them not to alert to the presence of smoke. The unit will sound if it receives a signal from an alarm in the same interconnected system. Once power is restored, a latched unit will sound an alert, regardless of the presence of smoke or carbon monoxide, until power to the alarm is completely removed.



It involves Kidde residential smoke alarms with model number i12010S manufactured between Dec. 18, 2013 and May 13, 2014, and combination smoke/CO alarms with model number i12010SCO manufactured between Dec. 30, 2013 and May 13, 2014 and model number KN-COSM-IBA manufactured between Oct. 22, 2013 and May 13, 2014. Kidde discovered the issue during an internal quality check. There have been no incidents reported, but due to our commitment to quality and safety, Kidde has taken action out of an abundance of caution. We have corrected the issue on future models, and are working with customers to obtain all affected units currently in stock.



See product safety notice placard (pdf) to help you identify recalled models.



For more information please contact Kidde at 1-844-553-9011 or www. Kidde. com.



March 26, 2012

9-1-1 Scam Alert



Residents in Washington and other states have reported receiving calls from someone requesting money for 9-1-1 services. The caller claims that residents must pay a fee to register their house in a 9-1-1 database so first responders can locate the home in an emergency. The caller also requests names and medical information from the residents.



This is a scam. 9-1-1 services are funded through dedicated 9-1-1 excise taxes on telephone bills and by other local government funds.  Any request for 9-1-1 funds over the phone is a fraud, and residents who receive these calls should hang up and report the suspicious call to their local police or sheriff’s non-emergency phone number.



For Port Ludlow residents, this phone number is 360-385-3831. The website for the Jefferson County Sheriff's Office is: http://www. jeffersonsheriff. org/



February 23, 2012

Meijer Recalls Touch Point Fan Heaters Due to Fire, Shock Hazards



On February 22, 2012, the U. S. Consumer Product Safety Commissioned announced a voluntary recall of Touch Point Forced Air Heaters sold at Meijer stores in Illinois, Indiana, Kentucky, Michigan and Ohio from September 2011 through November 2011 for about $20. Exposed and unshielded electrical components can cause the heater to overheat and melt, posing fire and electrical shock hazards.



January 12, 2012

Carruth Candleholder Collection Tea Light Candles Recalled Due to Fire Hazard



The tea light can burn with an excessive flame height, posing a fire hazard to consumers. The recalled tea lights were sold as part of the Carruth Candleholder Collection sets. The Carruth candleholder sets are resin votive candle holders with a glass insert that holds a tea light. The stock number is printed on a label on the bottom of the candleholders. The tea lights are white. The following eight models and stock numbers are included in this recall: Butterfly, 17708; Smile, 17709; Sun, 17710; Roots of Love, 17711; Sunflower, 17712; Hummingbird, 17713; Bunny, 17714; Friendship, 17715. Sold by: Home decorating and gift stores nationwide from January 2010 to November 2011 for about $14.

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The information in this section is provided as a public service of Port Ludlow Fire & Rescue. In the case of product recalls, please follow the link(s) in the notice for more information about recalled product(s). Links will open in a new browser window or tab.