Recalls and Product Safety Alerts
Our Product Safety Team proactively investigates and addresses reported safety complaints and incidents to ensure customer protection from potential product-related safety risks. We closely monitor public recall alert websites and receive notifications from vendors and sellers. Upon discovering a product recall, we immediately halt affected product offerings, and promptly inform both customers and sellers involved about the recall. For more information visit our Safety Information, Recalls and Legal Notices Page .
Search for recalls and alerts
Please, note that this list includes public alerts starting from 2024. This list may not be exhaustive and it only includes alerts for products sold on Amazon.
September 12, 2024
About 866,000 AirJet and HydroJet Spa Pumps Recalled Due to Fire Hazard; One Death Reported; Manufactured by Bestway and Sold with SaluSpa, Coleman, and Hydro-Force Spa Liners
September 12, 2024
GOETAS Pool Drain Covers Recalled Due to Entrapment Hazard; Violation of the Virginia Graeme Baker Pool and Spa Safety Act; Sold Exclusively on Amazon.com by GOETAS
September 12, 2024
MJKSARE High Chairs Recalled Due to Entrapment and Fall Hazards; Violation of Federal Regulation for High Chairs; Imported by Worldwide Windows; Sold Exclusively on Amazon.com
September 12, 2024
Intellio Toys Recalls Bright Builder Fort Kits Due to Battery Ingestion Hazard; Violation of Federal Regulations for Battery-Operated Toys
September 12, 2024
Class 2 Device Recall Medline
September 12, 2024
FDA Adds Warning About Rare Occurrence of Serious Liver Injury with Use of Veozah (fezolinetant) for Hot Flashes Due to Menopause. Stop Medicine if Signs and Symptoms of Liver Injury Occur - Drug Safety Communication
September 12, 2024
Class 2 Device Recall Medline
September 12, 2024
Petzl America Recalls GYM, PANDION and PANJI Climbing Harnesses Due to Fall Hazard
September 11, 2024
https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=209513
September 8, 2024
- PUBLIC RECALL TITLE: Class 1 Device Recall somat Space Infusion System/ Large Volume Pump
September 8, 2024
Chrysler (FCA US, LLC) is recalling certain MOPAR anti-lock braking system (ABS)-Disabled Electronic Stability Control/FMVSS 126
September 7, 2024
Class 2 Device Recall SolM Syringes with exchangeable needles
September 7, 2024
Class 2 Device Recall SOLM standard slip tip syringe without needle
September 7, 2024
Class 2 Device Recall SOLM Syringes with Low Dead Space
September 7, 2024
Class 2 Device Recall SolM Syringes with Fixed Needles
September 7, 2024
Class 2 Device Recall Medline
September 7, 2024
Disabled Electronic Stability Control/FMVSS 126
September 5, 2024
Niitakaya USA Inc. Issues Allergy Alert on Undeclared Allergen of Fish (Bonito) in #3700 Shiso Katsuo Ninniku/#3701 Miso Katsuo Ninniku
September 5, 2024
Delta Cycle Recalls Ceiling Hoists with Straps Due to Injury Hazard
September 4, 2024
Smiths Medical Issues Urgent Medical Device Notification Informing Customers of a Potential Issue with Certain Bivona® Tracheostomy Tubes
Further information on alerts can be accessed by clicking the links.
