This recall involves updating instructions for using 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 Device Description: Streamline Bloodline…
Recall Alert: Baxter Permanently Removes Life2000 Ventilation System
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 Product Product Name: Life2000 Ventilation System Product Code UDI-DI Number Product Code on Shipping Carton Product…
Wegmans Recalls Locatelli Grated Pecorino Romano Cheese Due to Possible Health Risk
Summary Company Announcement Date: November 26, 2025 FDA Publish Date: November 26, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential presence of Listeria monocytogenes. Company Name: Wegmans Food Markets, Inc. Brand Name: Brand Name(s) Product Description: Product Description Grated Pecorino Romano Cheese Company Announcement Rochester, N.Y. – Wegmans Food…
The Ambriola Company Issues Recall of Cheese Products Because of Listeria Health Risk
Summary Company Announcement Date: November 25, 2025 FDA Publish Date: November 26, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential to be contaminated with Listeria monocytogenes Company Name: The Ambriola Company Brand Name: Brand Name(s) Ambriola, Locatelli, Member’s Mark, Pinna, and Boar’s Head Product Description: Product Description Company…
Prairie Farms Announces Recall of Prairie Farms Gallon Fat Free Milk
Summary Company Announcement Date: November 25, 2025 FDA Publish Date: November 26, 2025 Product Type: Food & Beverages Contaminants Reason for Announcement: Recall Reason Description May contain food-grade cleaning agents Company Name: Prairie Farms Brand Name: Brand Name(s) Prairie Farms Product Description: Product Description Fat Free Milk Company Announcement EDWARDSVILLE, IL, November 25, 2025 —…
Silvestri Sweets Issues Voluntary Allergy Alert on Undeclared Pecan and Wheat in Cookie Butter Holiday Bark and Pecan, Cranberry & Cinnamon Holiday Bark
Summary Company Announcement Date: November 26, 2025 FDA Publish Date: November 26, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared pecans and wheat Company Name: Silvestri Sweet, Inc. Brand Name: Brand Name(s) Product Description: Product Description Bark candy with nuts and fruit Company Announcement Silvestri Sweets Inc. of Geneva,…
Recall Alert: BALT USA Removes MEGA Ballast Distal Access Platform
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 Products Product Names: MEGA Ballast Distal Access Platform (originally cleared as Next Generation Access Platform) Model…
MAMTAKIM Inc Recalls Dried Whole Smelts Salted (KORUSHKA) Because of Possible Health Risk
Summary Company Announcement Date: November 25, 2025 FDA Publish Date: November 25, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential to be contaminated with Clostridium botulinum. Company Name: Mamtakim, Inc. Brand Name: Brand Name(s) Product Description: Product Description Dried Whole Salted Smelt, Mullet, Goby Company Announcement MAMTAKIM Inc,…
Recall Alert: Max Mobility/Permobil Removes All SpeedControl Dials Used with SmartDrive MX2+ Power Assist Devices
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 Product Product Name: SpeedControl Dial used with SmartDrive MX2+ Power Assist Device Part Numbers: MX2-3DCK, MX2-3DC,…
Early Alert: Large Volume Pump Primary Administration Set Reverse Flow Issue from Fresenius Kabi
This Early Alert communication is part of the Communications Pilot to Enhance the Medical Device Recall Program. The FDA has become aware of a potentially high-risk 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 Fresenius Kabi has…