Biomet, Inc.: Medical Device Recalls in 2024

According to to data from the FDA, there were 3 medical device recalls made by Biomet, Inc. in 2024. See the details of the recalls below.

You can see similar recalls for other firms.

• JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357
• RingLoc Bi-Polar Hip System Acetabular Cup, 41 mm Outer Diameter - Used in hip hemi-arthroplasty Item Number: 11-165206
• Vanguard Knee System AS Tibial Bearing / DCM ArCom, 12 MM X 75 MM; Model Number 189082. The product is placed into a foil pouch with protective packaging in the form of a polyurethane bag, and sealed closed (inner barrier). The inner barrier is then placed into a PETG tray and sealed with Tyvek lid stock (outer barrier). The sealed double barrier system is placed into a paperboard carton with an IFU and label/indicator dots applied to the carton.