Summary Company Announcement Date: March 17, 2025 FDA Publish Date: March 18, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential Contaminant – Wood Company Name: Nestle USA Brand Name: Brand Name(s) Stouffer’s Product Description: Product Description Frozen meals Company Announcement ARLINGTON, VA., March 17, 2025 — Nestlé USA is initiating…
Embolization Device Recall and Correction: Medtronic Removes Unused 027 Compatible Pipeline Vantage Embolization Device with Shield Technology, Updates Use Instructions for 021 Compatible Pipeline Vantage Embolization Devices due to Increased Risk of Incomplete Wall Apposition and Braid Deformation
The FDA has identified this recall as the most serious type.This recall involves: removing the Pipeline Vantage 027 device models from where they are used or sold updating instructions for using the Pipeline Vantage 021 device models Affected Product Product Names: Removal of unused: Pipeline Vantage Embolization Device with Shield Technology, 027 Compatible (Pipeline Vantage…
Seabear Company Recalls Smoked Salmon Chowder and Alehouse Clam Chowder Because of Possible Health Risk
Summary Company Announcement Date: March 15, 2025 FDA Publish Date: March 15, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential contamination with Clostridium botulinum Company Name: Seabear Company Brand Name: Brand Name(s) Product Description: Product Description Alehouse Clam Chowder and Smoked Salmon Chowder Company Announcement SeaBear Company of Anacortes, Washington…
Disruptions in Availability of Hemodialysis Bloodlines – Letter to Health Care Providers
March 14, 2025 The U.S. Food and Drug Administration (FDA) is aware that the U.S. is experiencing interruptions in the supply of hemodialysis bloodlines because of recent supplier issues. The disruption in supply of this device is expected to impact patient care and as such may require adjustments to the clinical management of patients receiving…
C.H. Guenther & Son LLC Issues Allergy Alert on Undeclared Egg in “365 Whole Foods Market Small Bites Macaroni & Cheese”
Summary Company Announcement Date: March 14, 2025 FDA Publish Date: March 14, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared eggs Company Name: C.H. Guenther & Son LLC Brand Name: Brand Name(s) 365 Whole Foods Market Product Description: Product Description Small Bites Macaroni & Cheese Company Announcement C.H. Guenther &…
Har Maspeth Corp Issues Allergy Alert on Undeclared Eggs in “Jinga Glass Noodles w/ Vegetables (Japche)”
Summary Company Announcement Date: March 14, 2025 FDA Publish Date: March 14, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared eggs Company Name: HAR Maspeth Corp Brand Name: Brand Name(s) Product Description: Product Description Glass noodles with vegetables Company Announcement HAR Maspeth Corp, Maspeth NY, is recalling its 8 ounce…
Dr. Reddy’s Issues a Nationwide Recall of Levetiracetam in 0.75% Sodium Chloride Injection 1,000 mg/100 mL, in the U.S., Due to Mislabeling of Infusion Bag
Summary Company Announcement Date: March 13, 2025 FDA Publish Date: March 13, 2025 Product Type: Drugs Reason for Announcement: Recall Reason Description Mislabeling of infusion bag Company Name: Dr. Reddy’s Laboratories Ltd. Brand Name: Brand Name(s) Dr. Reddy’s Product Description: Product Description Levetiracetam in Sodium Chloride Injection Company Announcement Dr. Reddy’s Laboratories Ltd. (BSE: 500124,…
Smiths Medical Issues Urgent Medical Device Correction Informing Customers of a Potential Issue with Certain Sizes of Intubation ORAL/NASAL Endotracheal Tubes Being Smaller Than Expected
Summary Company Announcement Date: March 07, 2025 FDA Publish Date: March 10, 2025 Product Type: Medical Devices Reason for Announcement: Recall Reason Description Diameter of Device Smaller than Expected Company Name: Smiths Medical Brand Name: Brand Name(s) Product Description: Product Description Intubation Oral/Nasal Endotracheal Tubes Company Announcement MINNEAPOLIS, MN. March 7, 2025 – Smiths Medical…
New Age International Recalls Daily Veggies Brand Enoki Mushroom Due to Possible Health Risk
Summary Company Announcement Date: March 11, 2025 FDA Publish Date: March 12, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Listeria monocytogenes Company Name: New Age International Inc. Brand Name: Brand Name(s) Daily Veggies Product Description: Product Description Enoki Mushroom Company Announcement New Age International Inc of Brooklyn, NY…
Immune Globulin Intravenous (IGIV) and Immune Globulin Subcutaneous (IGSC): Voluntary Lot Withdrawals – Due to Increased Reports of Allergic/Hypersensitivity Reactions
AUDIENCE: Patient, Health Professional, Pharmacy, Immunology ISSUE: As a precautionary measure, the following lots of Immune Globulin Intravenous (IGIV) and Immune Globulin Subcutaneous (IGSC) have been voluntarily withdrawn by the manufacturers due to a higher rate of allergic/hypersensitivity type reactions, some of which were considered medically significant. Product Lot Date of Voluntary Withdrawal Expiration Date …