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…

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…

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…

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.

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

Early Alert: Aspiration System Issue from Calyxo

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program

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

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…

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…