Early Alert: Convenience Kit Issue from American Contract Systems

CDRH is issuing this Early Alert to notify the public of a potentially high-risk device issue. The FDA will keep the public informed and update this web page as significant new information becomes available.   Affected Product The FDA is aware that American Contract Systems has issued a letter to affected customers recommending certain angiographic…

Early Alert: Convenience Kit Issue from Medical Action Industries

CDRH is issuing this Early Alert to notify the public of a potentially high-risk device issue. The FDA will keep the public informed and update this web page as significant new information becomes available.  Affected Product The FDA is aware that Medical Action Industries has issued a letter to affected customers recommending certain angiographic syringes…

Liquid Blenz Corp. Recalls Product Due to Possible Health Risk

Summary Company Announcement Date: April 06, 2026 FDA Publish Date: April 14, 2026 Product Type: Food & Beverages Carbonated Soft Drinks Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness -Botulism Company Name: Liquid Blenz Corp Brand Name: Brand Name(s) Good Brain Tonic Product Description: Product Description Good Brain Tonic 16 oz &…

Early Alert: Sizing Catheter Issue from Cook Medical

Affected Product The FDA is aware that Cook Medical has issued a letter to affected customers recommending certain sizing catheters be removed from where they are used or sold. The affected devices are: Centimeter Sizing Catheters Aurous Centimeter Sizing Catheters Beacon Tip Centimeter Sizing Catheters The full list of affected product lots can be found here.   What…

Early Alert: Convenience Kit Issue from AVID Medical

CDRH is issuing this Early Alert to notify the public of a potentially high-risk device issue. The FDA will keep the public informed and update this web page as significant new information becomes available.   The FDA is aware that AVID Medical has issued an Urgent Medical Device Recall Notification to affected customers recommending certain…

Blaine Labs, Inc Issues Voluntary Nationwide Recall of Wound Care Gel Products Due to Microbial Contamination

Summary Company Announcement Date: April 08, 2026 FDA Publish Date: April 08, 2026 Product Type: Drugs Reason for Announcement: Recall Reason Description Products were found to contain Lysinibacillus fusiformis, an environmental organism Company Name: Blaine Labs, Inc. Brand Name: Brand Name(s) Revitaderm, Tridergel Product Description: Product Description Antiseptic wound care gel bottles and tubes Company…