Please be aware, this recall is a correction, not a product removal. The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Product Names: Panorama 1.0T HFO Product Codes: LNH Model Numbers: 781250 and 781350 Distribution Dates:…
Insight Pharmaceuticals Issues Voluntary Nationwide Recall of Americaine® 20% Benzocaine Topical Anesthetic Spray Due to the Presence of Benzene
Summary Company Announcement Date: December 22, 2023 FDA Publish Date: December 22, 2023 Product Type: Drugs Reason for Announcement: Recall Reason Description Presence of benzene Company Name: Insight Pharmaceuticals Brand Name: Brand Name(s) Americaine Product Description: Product Description Benzocaine Topical Anesthetic Spray Company Announcement TARRYTOWN, N.Y., Dec. 22, 2023 (GLOBE NEWSWIRE) — Insight Pharmaceuticals, a…
Hospira, Inc. Issues A Voluntary Nationwide Recall For One Lot of Bleomycin for Injection, USP 15 Units Single Dose ONCO-TAIN™ Glass Fliptop Vial Due To The Potential For Presence of Glass Particulate Matter
Summary Company Announcement Date: December 21, 2023 FDA Publish Date: December 22, 2023 Product Type: Drugs Reason for Announcement: Recall Reason Description Presence of Glass Particulate Matter Company Name: Hospira, Inc. Brand Name: Brand Name(s) Product Description: Product Description Bleomycin for Injection, USP 15 Units Single Dose ONCO-TAIN™ Glass Fliptop Vial Company Announcement FOR IMMEDIATE…
ResMed Notifies Customers About Updated Instructions and Labeling for Masks with Magnets Due to Potential Interference with Certain Medical Devices
Summary Company Announcement Date: December 20, 2023 FDA Publish Date: December 21, 2023 Product Type: Medical Devices Reason for Announcement: Recall Reason Description Potential for magnetic interference near certain implants and medical devices Company Name: ResMed Brand Name: Brand Name(s) Product Description: Product Description Masks with magnets Company Announcement ResMed’s masks with magnets are safe…
Medline Industries, LP. Issues a Voluntary Nationwide Recall of Various Lots of Tracheostomy Care and Cleaning Trays
Summary Company Announcement Date: December 20, 2023 FDA Publish Date: December 20, 2023 Product Type: Medical Devices Reason for Announcement: Recall Reason Description Device & Drug Safety – Potential Component Defect Company Name: Medline Industries, LP Brand Name: Brand Name(s) Product Description: Product Description Tracheostomy Care and Cleaning Trays Company Announcement Northfield, Ill., Dec. 20,…
Govvi WOW! contains hidden drug ingredient
[12-21-2023] The Food and Drug Administration is advising consumers not to purchase or use Govvi WOW!, a product promoted and sold for weight loss on various websites, including www.ebay.com and possibly in some retail stores. FDA laboratory analysis confirmed that Govvi WOW! contains undeclared DMAA (1,3-dimethylamylamine or methylhexanamine). The dietary supplement industry often refers to…
Astor Chocolate Corporation Issues Allergy Alert on Undeclared Coconut in Burnt Caramel Bars
Summary Company Announcement Date: December 21, 2023 FDA Publish Date: December 21, 2023 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential Allergen – Undeclared Coconut Company Name: Astor Chocolate Corporation Brand Name: Brand Name(s) Product Description: Product Description Burnt Caramel Candy Bars Company Announcement Astor Chocolate Corporation of Lakewood, New Jersey…
Busse Hospital Disposables Issues Nationwide Recall of Kits/Trays Containing Sterile Water Based Products Under Recall by Nurse Assist
Summary Company Announcement Date: December 19, 2023 FDA Publish Date: December 20, 2023 Product Type: Medical Devices Reason for Announcement: Recall Reason Description Device & Drug Safety – Potential Lack of Sterility Company Name: Busse Hospital Disposals Brand Name: Brand Name(s) Busse Hospital Disposals Product Description: Product Description Medical Device Kits and Trays Company Announcement…
RDK Corp (DBA Racine Danish Kringles) Issues Allergy Alert on Potential for Undeclared Pecans in 14oz Raspberry Kringle
Summary Company Announcement Date: December 19, 2023 FDA Publish Date: December 19, 2023 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared Allergen – Pecans Company Name: RDK Corp Brand Name: Brand Name(s) Racine Danish Kringles Product Description: Product Description Raspberry Kringle Danish Company Announcement Racine Danish Kringles of Racine, Wisconsin is…
Houdini, Inc. Recalls Gift Baskets with Quaker Oats Chewy Granola Bars Because of Possible Health Risk
Summary Company Announcement Date: December 19, 2023 FDA Publish Date: December 19, 2023 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Salmonella contamination Company Name: Houdini, Inc. Brand Name: Brand Name(s) Wine Country Gift Baskets Product Description: Product Description Gift Baskets with Quaker Chewy Granola Bars Company Announcement Wine…