[12-26-2023] The Food and Drug Administration is advising consumers not to purchase or use Wild Bull, a product promoted and sold for sexual enhancement on various websites, including www.amazon.com, and possibly in some retail stores. FDA laboratory analysis confirmed that Wild Bull contains nortadalafil. Nortadalafil is structurally similar to tadalafil, the active ingredient in the…
TO THE MOON contains hidden drug ingredient
[12-26-2023] The Food and Drug Administration is advising consumers not to purchase or use TO THE MOON, a product promoted and sold for sexual enhancement on various websites, including www.amazon.com, and possibly in some retail stores. FDA laboratory analysis confirmed that TO THE MOON contains sildenafil, the active ingredient in the FDA-approved prescription drug Viagra,…
World Variety Produce, Inc. Recalls Kimchi Hot Because of Possible Health Risk
Summary Company Announcement Date: December 22, 2023 FDA Publish Date: December 26, 2023 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared Fish Company Name: World Varity Produce, Inc. Brand Name: Brand Name(s) World Varity Produce, Inc. Product Description: Product Description Melissa’s Hot Kimchi Company Announcement FOR IMMEDIATE RELEASE – December 22,…
Hospira, Inc. Issues A Voluntary Nationwide Recall For 4.2% Sodium Bicarbonate Injection, 8.4% Sodium Bicarbonate Injection, and Atropine Sulfate Injection Due to the Potential Presence of Glass Particulate Matter
Summary Company Announcement Date: December 21, 2023 FDA Publish Date: December 26, 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 4.2% Sodium bicarbonate injection, 8.4% Sodium bicarbonate injection, Atropine sulfate injection Company Announcement FOR IMMEDIATE RELEASE…
Recall of Certain Saline and Sterile Water Medical Products Associated with Nurse Assist: FDA Safety Communication
Español Update: December 19, 2023 Additional Related Recalls of Saline and Sterile Water Medical Products Associated with Nurse Assist In direct response to the Nurse Assist, LLC recall on November 6, 2023, distributors of Nurse Assist water-based medical products and manufacturers of kits and trays that contain Nurse Assist recalled products are initiating voluntary recalls. …
Tampa Bay Fisheries, Inc. Dover, Florida is Voluntarily Recalling 1 Lot of 365 Whole Foods Market Beer Battered Pollock Fillets and 2 Lots of 365 Beer Battered Cod Fillet Due to an Undeclared Soy Allergen
Summary Company Announcement Date: December 22, 2023 FDA Publish Date: December 23, 2023 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared Soy Company Name: Tampa Bay Fisheries, Inc. Brand Name: Brand Name(s) 365 WHOLE FOODS MART Product Description: Product Description Beer Battered Pollock and Cod Fillets Company Announcement TAMPA BAY FISHERIES,…
Philips North America LLC Recalls Panorama 1.0T HFO due to a Risk of Explosion During a Quench Procedure Caused by Excessive Pressure Buildup of Helium Gas
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…