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. Please be aware, this recall is a correction, not a product removal. Recalled Product Product Names: Olympus bronchofiberscopes and bronchovideoscopes Product Codes: See Recall Database Entry Model Numbers: See full…
T XTRA Strength Test Booster contains hidden drug ingredient
[12-26-2023] The Food and Drug Administration is advising consumers not to purchase or use T XTRA Strength Test Booster, a product promoted and sold for sexual enhancement and as an energy booster on various websites, including www.amazon.com, and possibly in some retail stores. FDA laboratory analysis confirmed that T XTRA Strength Test Booster contains tadalafil,…
Sustain® contains hidden drug ingredients
[12-26-2023] The Food and Drug Administration is advising consumers not to purchase or use Sustain®, 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 Sustain® contains tadalafil and avanafil, the active ingredients in the FDA-approved prescription drugs Cialis and Stendra,…
Schwinnng contains hidden drug ingredient
[12-26-2023] The Food and Drug Administration is advising consumers not to purchase or use Schwinnng, 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 Schwinnng contains nortadalafil. Nortadalafil is structurally similar to tadalafil, the active ingredient in the FDA-approved prescription…
Wild Bull contains hidden drug ingredient
[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,…