This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it. The affected products and recommendations for what to do with the devices below have not changed. Affected…
Hometown Food Company Issues Allergy Alert on Undeclared Egg in Birch Benders 12oz Sweet Potato Pancake Mix
Summary Company Announcement Date: May 20, 2026 FDA Publish Date: May 21, 2026 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description May contain undeclared egg. Company Name: Hometown Food Company Brand Name: Brand Name(s) Birch Benders Product Description: Product Description Sweet Potato Pancake & Waffle Mix Company Announcement Chicago (May 20,…
Kettle Cuisine Issues Allergy Alert For Undeclared Shrimp In Whole Foods Market Kitchen Minestrone Soup
Summary Company Announcement Date: May 21, 2026 FDA Publish Date: May 21, 2026 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description May Contain Undeclared Shrimp Company Name: Kettle Cuisine Brand Name: Brand Name(s) Whole Foods Market Product Description: Product Description Minestrone Soup Company Announcement Kettle Cuisine of Lynn, MA is recalling…
Early Alert: Heart Pump Controller Issue from Abiomed
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 Abiomed has issued an Urgent Medical Device Recall (Correction) notice to affected customers recommending…
Thoracic Stent Graft Recall: Bolton Medical Removes Relay Pro System
The affected products and recommendations for what to do with the devices below have not changed. This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it. Affected…
Nassar Investments Recalls Malazi Tahina Due to Salmonella Contamination
Summary Company Announcement Date: May 18, 2026 FDA Publish Date: May 18, 2026 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Due to contamination of Salmonella Company Name: Nassar Investment Co., LLC. Brand Name: Brand Name(s) Product Description: Product Description Company Announcement RALEIGH, NC – MAY 19, 2026 – Nassar…
Sugar Foods Issues Recall of Specific Lots of Kroger Homestyle Cheese Garlic Croutons Due to Possible Health Risk
Summary Company Announcement Date: May 15, 2026 FDA Publish Date: May 18, 2026 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Due to potential for Salmonella contamination. Company Name: Sugar Foods, LLC. Brand Name: Brand Name(s) Product Description: Product Description Cheese and Garlic Croutons Company Announcement WESTLAKE VILLAGE, CA –…
Blackstone Products Recalls Parmesan Ranch Seasoning Because of Possible Salmonella Health Risk
Summary Company Announcement Date: May 15, 2026 FDA Publish Date: May 15, 2026 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Salmonella Company Name: Blackstone Products Brand Name: Brand Name(s) Blackstone Product Description: Product Description Parmesan Ranch seasoning Company Announcement Blackstone Products of Providence, Utah is…
Straus Family Creamery Voluntarily Recalls Select Flavors of Organic Ice Cream Due to Potential Presence of Foreign Material
Summary Company Announcement Date: May 14, 2026 FDA Publish Date: May 15, 2026 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Presence of metal fragments Company Name: Straus Family Creamery Brand Name: Brand Name(s) Straus Family Creamery Product Description: Product Description Various Ice Cream Products, pint and quart sizes Company Announcement May…
Early Alert: Anesthesia Machine Issue from Draeger, Inc.
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 Draeger, Inc. has issued a letter to affected customers recommending certain anesthesia Machine be…