The FDA has since determined that this device may cause temporary or reversible health problems, or—though unlikely—serious health problems. 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. Affected Product The FDA is aware that…
Catheter Recall: Medline Industries Removes Reprocessed Electrophysiology and Ultrasound Catheters
The affected products below have 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. Medline Industries has issued an expansion to this recall. Affected Product…
Frito-Lay Issues Voluntary Allergy Alert on Undeclared Milk in Miss Vickie’s Spicy Dill Pickle Potato Chips
Summary Company Announcement Date: March 03, 2026 FDA Publish Date: March 04, 2026 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared milk allergen Company Name: Frito-Lay Brand Name: Brand Name(s) Miss Vickie’s Product Description: Product Description Spicy Dill Pickle Potato Chips Company Announcement Plano, Texas – March 3, 2026 – Frito-Lay…
Savannah Bee Company Recalls Honey BBQ Sauce-Mustard Due to Undeclared Wheat and Soy
Summary Company Announcement Date: February 27, 2026 FDA Publish Date: February 27, 2026 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared wheat and soy Company Name: Savannah Bee Company Brand Name: Brand Name(s) Savannah Bee Company Product Description: Product Description Company Announcement SAVANNAH, GA 2-27-2026 – Savannah Bee Company is…
USA LESS Co. is Recalling Rhino Choco VIP 10X Due to Undeclared Tadalafil
Summary Company Announcement Date: February 27, 2026 FDA Publish Date: February 27, 2026 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared Tadalafil Company Name: USA LESS Co. Brand Name: Brand Name(s) RHINO CHOCO VIP 10X Product Description: Product Description Company Announcement BROOKLYN, N.Y., Feb. 27, 2026 /PRNewswire/ — USALESS.COM is recalling…
Stent Recall: Boston Scientific Removes Certain AXIOS Stents and Electrocautery-Enhanced Delivery Systems
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…
Early Alert: Heart Pump Purge Cassette 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 a letter to affected customers recommending certain Impella Purge Cassettes and…
GO Raw LLC. Expands Voluntary Recall of Quest Diet Cat Food Products Due to Low Thiamine Levels and Enacts Stop Sale of All Quest Products
Summary Company Announcement Date: February 26, 2026 FDA Publish Date: February 26, 2026 Product Type: Animal & VeterinaryFood & Beverages Pet Food Reason for Announcement: Recall Reason Description May contain low levels of thiamine (Vitamin B1) Company Name: Go Raw LLC. Brand Name: Brand Name(s) Product Description: Product Description Cat Food Chicken Recipe Freeze Dried…
Infusion Pump Software Correction: Fresenius Kabi Issues Correction for Ivenix Large Volume Pump Software
This recall involves correcting certain devices and does not involve removing them 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 without correction. Affected Product The FDA is aware that Fresenius Kabi…
Lockout Supplements Issues Voluntary Nationwide Recall of Boner Bears Chocolate Syrup Due to Undeclared Sildenafil
Summary Company Announcement Date: February 25, 2026 FDA Publish Date: February 25, 2026 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared Sildenafil Company Name: Lockout Supplements Brand Name: Brand Name(s) Boner Bears Product Description: Product Description Chocolate syrup Company Announcement FOR IMMEDIATE RELEASE: 02/252026-McKinney, Texas, Lockout Supplements is voluntarily recalling all…