Important: CPSC Recall Remedy Notice Due to COVID-19
Due to the extraordinary circumstances surrounding COVID-19, some of the remedies identified in recall press releases may not be available at this time. Consumers should check with recalling firms for further details.
It is important to remember that CPSC and recalling firms urge consumers not to use recalled products.
Consumers should immediately stop using the recalled HR Platform Frames and contact Global Home Imports to receive a free repair kit with metal clips to strengthen the frame. Global Home Imports will ship a kit directly to consumers free of charge.
Consumers should immediately stop using the recalled mattresses and contact HOFISH to receive a free fitted cover to put on the mattress to bring it into compliance with the federal standard.
Consumers should immediately stop using the recalled candles, carefully cut all three wicks as short as possible to prevent the candles from being used and discard the product. Melaleuca has contacted all known purchasers directly about the recall and refund.
Consumers should immediately stop riding the recalled motorcycles and contact an authorized KTM or Husqvarna Motorcycles dealer, respective of their motorcycle brand, to schedule a free repair. KTM and Husqvarna Motorcycles are contacting all known purchasers directly.
Consumers should immediately stop using the recalled seminar tables and contact Lifetime Products for a free repair bracket.
Consumers should immediately stop using the recalled Jennings counter and bar stools and contact Hillsdale Furniture for a free repair kit.
Consumers should immediately stop using the recalled vehicles and contact a Polaris dealer to schedule a free repair. Polaris is notifying all dealers and contacting registered owners directly.
About 33,954 (In addition, 1,492 units were sold in Canada)
Polaris at 800-765-2747 from 7 a.m. to 7 p.m. CT Monday through Friday or online at www.polaris.com and click on “Off Road Safety Recalls” or https://www.polaris.com/en-us/off-road-recalls/ to check your vehicle identification number “VIN” or go to “Product Safety Recalls” page to see if your vehicle is included in any recalls or online at https://www.polaris.com/en-us/recalls/off-road/.
Consumers should immediately stop using their recalled Cabina Bunk Beds until they have inspected their beds to determine whether the screws that hold the bed’s foundation to the guardrails are tightly in place. Casa Kids is contacting all purchasers directly with detailed instructions on how to inspect and repair their bunk beds. Casa Kids will immediately send a new set of screws to any consumers who alert Casa Kids that their bed’s guardrails are not tightly in place.
Casa Kids collect at 718-694-0272 from 9 a.m. to 5 p.m. ET Monday through Friday, email at email@example.com, or online at www.casakids.com/pages/productrecall for instructions on how to inspect and repair the bunk bed, or at www.casakids.com and click on “Product Recall,” located in the page’s footer in the “Additional Information” column for more information.
Consumers should immediately stop using the recalled bicycles and contact their local Haro Bicycles dealer for a free inspection, and repair or replacement of the fork and compression plug.
Consumers should immediately store the recalled medications in a safe location out of reach of children and contact Dr. Reddy’s for a full refund.
Dr. Reddy’s toll-free at 888-375-3784 from 8 a.m. to 8 p.m. ET Monday through Friday, or online at www.drreddys.com and click on “Recall” for more information. Report incidents related to children accessing or ingesting these prescription medications to www.SaferProducts.gov. Report adverse events, medication errors, and quality problems related to the use of these products to FDA’s MedWatch Adverse Event Reporting Program either online at www.fda.gov/medwatch/report.htm, download the form at www.fda.gov/MedWatch/getforms.htm or call 800-332-1088 to request a reporting form, then complete and submit by regular mail, and return to the address on the pre-addressed form, or submit by fax to 800-FDA-0178.