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 .

To see if any of your past orders have been recalled, visit Your Recalls and Product Safety Alerts

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.

July 18, 2024

Class 2 Device Recall Infusomat Pump Set

July 18, 2024

Class 2 Device Recall Infusomat

July 18, 2024

Class 2 Device Recall Infusomat

July 18, 2024

Class 2 Device Recall Outlook

July 18, 2024

BISSELL Recalls More Than 3 Million Steam Shot Handheld Steam Cleaners Due to Burn Hazard

July 18, 2024

Class 2 Device Recall Infusomat

July 18, 2024

Class 2 Device Recall Infusomat

July 18, 2024

Class 2 Device Recall Outlook

July 18, 2024

[B. Braun Medical] - [Infusomat UNIV. 15 DR PUMP SET, 1.2 FIL, 2 CRSTE/ASV]

July 18, 2024

CFMOTO Recalls ZFORCE 950 Recreational Off-Highway Vehicles (ROVs) Due to Crash and Tip-Over Hazards

July 17, 2024

GURU INC. Issues Voluntary Nationwide Recall of Infla-650 Herbal Dietary Supplement Capsules Due to Hidden Drug Ingredients

July 17, 2024

Class 2 Device Recall SURGICEL FIBRILLAR Absorbable Hemostat

July 17, 2024

Class 2 Device Recall Infusomat

July 17, 2024

Class 2 Device Recall SURGICEL FIBRILLAR Absorbable Hemostat

July 17, 2024

Class 2 Device Recall Infusomat

July 17, 2024

Class 2 Device Recall Infusomat

July 17, 2024

Class 2 Device Recall Infusomat

July 16, 2024

SoloVital.com Issues Voluntary Nationwide Recall of Umary Acido Hialuronica, Suplemento Alimenticio 850 mg Capsules Due to the Presence of Undeclared Drug Ingredients: Diclofenac and Omeprazole

July 13, 2024

Class 2 Device Recall Glide Knee Walker

July 13, 2024

Class 2 Device Recall Glide Knee Walker

Further information on alerts can be accessed by clicking the links.