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FDA
March 26, 2025
Safe Use of Megadyne Mega 2000 and Mega Soft Patient Return Electrodes – Letter to Health Care Providers
Read the FDA’s recommendations related to four recalls of Megadyne Mega 2000 and Mega Soft patient return electrodes for patient…
FDA
March 25, 2025
Henkel Capital S.A. de C.V. Recalls Tec Italy Totale Shampoo Due to Potential Health Risk
Henkel Capital S.A. de C.V. (“Henkel”) of Mexico is voluntarily recalling 1,068 units of its Tec Italy Shampoo Totale, as…
FDA
March 25, 2025
The Bakery Group Issues Allergen Alert on Undeclared Milk, Soy and Yellow FD&C #5 In Specific Bread and Hamburger Buns
The Bakery Group of Dallas, Tx is recalling 629 cases of Dense Brioche Pullman loaves, #654203 and 104 cases of…
FDA
March 25, 2025
Endotracheal Tube Recall: Smiths Medical Removes Intubation ORAL/NASAL Endotracheal Tubes Due to Smaller Than Expected Tube Diameter That May Cause Underventilation
ORAL/NASAL Endotracheal Tubes keep air flowing through a patient’s airway, but some tubes may be smaller in diameter than expected.
FDA
March 20, 2025
Update on Alert: Atherectomy Catheter System Issue from Bard Peripheral Vascular
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
FDA
March 20, 2025
Early Alert: Aspiration System Issue from Calyxo
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
FDA
March 20, 2025
Infusion Pump Software Correction: Becton, Dickinson and Company (BD) Issues Correction for BD Alaris Systems Manager and Care Coordination Engine Infusion Adapter Software Due to Risk for Outdated Automated Programming Requests to Load
Software from Alaris System Manager and CCE Infusion Adapter needs updates so outdated infusion information does not load to the…
FDA
March 20, 2025
Update on Alert: Infusion Pump Issue from Baxter Healthcare Corporation
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
FDA
March 19, 2025
Dessert Holdings Issues Allergy Alert on Undeclared Tree Nut Allergen in Favorite Day™ Gourmet New York Style Cheesecake 6oz/2ct
Dessert Holdings LLC is recalling Target brand Favorite Day™ Gourmet New York Style Cheesecake 6oz/2ct, Lot code 25028A1 000039133 UPC…
FDA
March 19, 2025
Implantable Port Recall: Smiths Medical Removes ProPort Plastic Implantable Ports Due to Manufacturing Error that May Cause Separation
A manufacturing error may cause ProPort Plastic Implantable Ports, which are used in patients who need repeat venous access for…
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