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.
August 2, 2026
Incorrect Breaker May Allow Conductor to Overheat
August 2, 2026
Antilock Braking System May Fail
August 1, 2026
Class 1 Device Recall Halyard
August 1, 2026
Class 2 Device Recall Quantum Rehab
August 1, 2026
Class 2 Device Recall Quantum Rehab
August 1, 2026
Lidl US Expands Recall of Eridanous Shortbread Cookies Due to Undeclared Wheat, Soy, Milk, Egg and Tree Nut (Coconut) Allergens
August 1, 2026
[Beckman Coulter Biomedical GmbH] - [REMISOL Advance with Software Version 2.5]
August 1, 2026
Class 2 Device Recall Quantum Rehab
August 1, 2026
Class 2 Device Recall Nerivio Infinity
August 1, 2026
Class 2 Device Recall WASPLab
August 1, 2026
Quantum Rehab recalls Q6 Edge 3 due to If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this occurs while not driving the wheelchair, the control system may crash and remain in pre-operational mode.
August 1, 2026
Class 2 Device Recall Quantum Rehab
August 1, 2026
Class 2 Device Recall Radial Jaw 4 Jumbo Biopsy Forceps
August 1, 2026
Class 2 Device Recall Quantum rehab
August 1, 2026
Class 1 Device Recall Halyard
August 1, 2026
Public Recall : Radial Jaw 4 Standard Capacity Biopsy Forceps due to Hazard: Contamination, Potential breach in sterile barrier of device packaging
August 1, 2026
Class 2 Device Recall Kingfisher Compact Individual First Aid Kit
August 1, 2026
Class 1 Device Recall Halyard
August 1, 2026
Class 2 Device Recall Quantum Rehab
August 1, 2026
Class 2 Device Recall munevo DRIVE
Further information on alerts can be accessed by clicking the links.
