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.

September 28, 2024

Class 2 Device Recall Healgen Series Reagent Strips for Urinalysis

September 27, 2024

Class 2 Device Recall CardinalHealth

September 26, 2024

Class 3 Device Recall Eakin Cohesive small seals

September 26, 2024

Incorrect Tire Identifcation Number/FMVSS 574

September 26, 2024

Liberty Hardware Recalls Multi-Grip Tub Safety Bars Due to Fall Hazard

September 26, 2024

Class 2 Device Recall CardinalHealth

September 25, 2024

Truly Good Foods Issues Allergy Alert on Undeclared Almonds and Cashews in Grabeez The Big Cheese Snack Mix 3.25 oz Cup

September 23, 2024

ANSWERS Pet Food Voluntarily Withdrawals Certain Limited Lots of Beef and Chicken Dog Foods Due to Potential Salmonella and Listeria

September 23, 2024

Class 2 Device Recall Good Vibrations

September 20, 2024

public recall tittle: Incomplete insertion of the patient connector of the Streamline Airless System Hemodialysis Bloodline to the Locksite may result in the potential for occlusion during prograde rinseback procedures. If the patient connector is not fully inserted into the Locksite, the internal septum may not open fully enough to prevent restrictions to flow. may cause delays in therapy while clinicians are forced to switch to retrograde flow method

September 20, 2024

123Herbals LLC (123Herbals.com) Issues Voluntary Nationwide Recall of Vail-Bon Jie Yang Wan Capsules Due to the Presence of Undeclared Dexamethasone and Chlorpheniramine

September 20, 2024

Class 2 Device Recall Hemodialysis Bloodlines

September 20, 2024

Class 2 Device Recall Safeguard US Operating LLC

September 20, 2024

KTM Services Inc. Issues Allergy Alert on Undeclared Milk in Cookies

September 20, 2024

Class 2 Device Recall Acceava Respiratory Strep A

September 20, 2024

Avole Inc. Issues Allergy Alert on Undeclared Fish in Bacalaitos Criollos Codfish Mix

September 20, 2024

HP Hood LLC Recalls Select Units of 96 oz Refrigerated Lactaid Milk Due to Possible Almond Allergen

September 19, 2024

Children’s Jewelry Sets Recalled Due to Risk of Lead and Cadmium Poisoning; Violations of the Federal Lead Content Ban and Federal Hazardous Substances Act; Sold Exclusively on Amazon.com by Newmemo

September 19, 2024

Wee Gallery Recalls Baby Tummy Time Gallery Due to Violation of the Federal Phthalates Ban

September 19, 2024

Ceither Adult Portable Bed Rails Recalled Due to Serious Entrapment and Asphyxia Hazards; Violation of Federal Regulations for Adult Portable Bed Rails; Sold Exclusively on Amazon.com by Inforce

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