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 4, 2027
SUPPLX.com Issues Voluntary Nationwide Recall of Business Pill and Branch Manager for Men Due to Undeclared Yohimbine
September 1, 2027
Class 2 Device Recall Medline
September 22, 2026
Otsuka ICU Medical LLC Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection, USP Due To a Product Mix-up with 10 mEq Potassium Chloride Injection
September 22, 2026
[Global Mix] [Niwali Tejocote Capsules and Niwali Tejocote Pieces]
September 20, 2026
Class 2 Device Recall VITEK 2 ASTN461 TEST KIT
September 20, 2026
Melissa & Doug Recalls Fire Truck Activity Board Toys Due to Risk of Serious Injury from Choking Hazard; Sold Exclusively at Target
September 19, 2026
Class 2 Device Recall Olympus EZDilate Endoscopic Balloon Dilator
September 19, 2026
Class 2 Device Recall Ingenia 3.0T
September 19, 2026
Class 2 Device Recall Ingenia 1.5T
September 19, 2026
Class 2 Device Recall Olympus BiCOAG Hemostasis Probe 10Fr Coaxial Connector
September 19, 2026
Class 2 Device Recall Achieva XR
September 19, 2026
Class 2 Device Recall Getinge PowerLED
September 19, 2026
Pearle Vision 1 day
September 19, 2026
Gias Foods, Inc. Recalls Bettergoods Authentic Italian Lemon Alfredo Fettuccine Because of Possible Health Risk
September 19, 2026
Class 2 Device Recall Olympus BiCOAG Hemostasis Probe 7Fr Coaxial Connector
September 19, 2026
Class 2 Device Recall Philips EPIQ Elite Diagnostic Ultrasound System
September 19, 2026
Class 2 Device Recall HomeFill Oxygen System
September 19, 2026
Class 2 Device Recall IQvitals Zone
September 19, 2026
Class 2 Device Recall SeaSpine Mariner Deformity
September 19, 2026
Class 2 Device Recall MR 5300
Further information on alerts can be accessed by clicking the links.
