Zimmer Biomet Recalls
875 recalls on record · January 20, 2016 to December 30, 2020 · Medical Devices
Recalls by year
16
17
18
19
20
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 125 13 mm x 280 mm, Item Number 814313280 Product Usage: Intended for the fixation o
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 125 13 mm x 260 mm, Item Number 814313260 Product Usage: Intended for the fixation o
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 125 13 mm x 180 mm, Item Number 814313180 Product Usage: Intended for the fixation o
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 125 11 mm x 460 mm, Item Number 814311460 Product Usage: Intended for the fixation o
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 125 11 mm x 440 mm, Item Number 814311440 Product Usage: Intended for the fixation o
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 125 11 mm x 420 mm, Item Number 814311420 Product Usage: Intended for the fixation o
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 125 11 mm x 380 mm, Item Number 814311380 Product Usage: Intended for the fixation o
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 125 11 mm x 360 mm, Item Number 814311360 Product Usage: Intended for the fixation o
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 125 11 mm x 340 mm, Item Number 814311340 Product Usage: Intended for the fixation o
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail 125 11mm x 180mm, Item Number 814311180 Product Usage: Intended for the fixation of fracture
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 125 9 mm x 460 mm, Item Number 814311460 Product Usage: Intended for the fixation of
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 125 9 mm x 440 mm, Item Number 814309440 Product Usage: Intended for the fixation of
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 125 9 mm x 380 mm, Item Number 814309380 Product Usage: Intended for the fixation of
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 125 9 mm x 360 mm, Item Number 814309360 Product Usage: Intended for the fixation of
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 125 9 mm x 340 mm, Item Number 814309340 Product Usage: Intended for the fixation of
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 125 9 mm x 320 mm, Item Number 814309320 Product Usage: Intended for the fixation of
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 125 9 mm x 300 mm, Item Number 814309300 Product Usage: Intended for the fixation of
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 125 9 mm x 260 mm, Item Number 814309260 Product Usage: Intended for the fixation of
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail 125 9 mm x 180 mm, Item Number 814309180 Product Usage: Intended for the fixation of frac
Hazard: There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
October 3, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Biomet Sports Medii cine Juggerknot Long Flex Drill Bit with Sleeve Nitinol intended to be used for soft tissue to bone
Hazard: Expiration date incorrectly listed on the label
October 3, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment, Model Number 185224 Intended for use in T
Hazard: The implant only has one bolt in the sterile package but it should have had two.
October 3, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Vanguard 360 Revision Knee System 63x 10mm Universal Tibial Block Augment, Model Number 185221 Intended for use in
Hazard: The implant only has one bolt in the sterile package but it should have had two.
October 3, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Zimmer Natural Nail Tibial Nail - Yellow 8.3mm, Model Number 47249534008 Product Usage - The Zimmer Natural Nail Syst
Hazard: The item is labeled as an 8.3mm, but it is actually a 12 mm.
September 26, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Gentle Thread PLGA Full Thread Interference Screw, 10x30mm, Item Number 905629
Hazard: The Gentle Thread PLGA Round Head, 7x20mm and the Gentle Thread PLGA Full Thread 10x30 have been commingled.
September 26, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Gentle Thread PLGA Round Head Interference Screw, 7x20mm, Item Number 905612
Hazard: The Gentle Thread PLGA Round Head, 7x20mm and the Gentle Thread PLGA Full Thread 10x30 have been commingled.
September 19, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus¿ Hip Fracture Nail Left 130¿ 15 mm x 360 mm, Item Number: 814615360
Hazard: The set screw is not able to advance or reverse from the original position in the nail.
September 19, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 460 mm, Item Number: 814613460
Hazard: The set screw is not able to advance or reverse from the original position in the nail.
September 19, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 440 mm, Item Number: 814613440
Hazard: The set screw is not able to advance or reverse from the original position in the nail.
September 19, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 420 mm, Item Number: 814613420
Hazard: The set screw is not able to advance or reverse from the original position in the nail.
September 19, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 400 mm, Item Number: 814613400
Hazard: The set screw is not able to advance or reverse from the original position in the nail.