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.
November 7, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls EBI Osteogen Implantable Bone Growth Stimulator The OsteoGen Implantable Bone Growth Stimulator is indicated in the
Hazard: Lack of adequate validation and controls to ensure that product cleanliness parameters were consistently met.
October 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail 125 9 mm x 165 mm, Item Number 816709165 Product Usage: Intended for the fixation of fract
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 Left 130 15 mm x 360 mm, Item Number 814615360 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 Left 130 11 mm x 400 mm, Item Number 814611400 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 Left 130 11 mm x 380 mm, Item Number 814611380 Product Usage: Intended for the fixation
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 Left 130 11 mm x 360 mm, Item Number 814611360 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 Left 130 9 mm x 360 mm, Item Number 814609360 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 130 13 mm x 360 mm, Item Number 814513360 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 130 11 mm x 400 mm, Item Number 814511400 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 130 11 mm x 360 mm, Item Number 814511360 Product Usage: Intended for the fixation
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 130 11 mm x 340 mm, Item Number 814511340 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 130 11 mm x 320 mm, Item Number 814511320 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 130 11 mm x 180 mm, Item Number 814511180 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 24, 2018Medical DevicesFDA
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 130 9 mm x 320 mm, Item Number 814509320 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 Left 125 13 mm x 360 mm, Item Number 814413360 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 Left 125 13 mm x 340 mm, Item Number 814413340 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 Left 125 13 mm x 260 mm, Item Number 814413260 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 Left 125 11 mm x 360 mm, Item Number 814411360 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 - Left 125 11mm x 340mm, Item Number 814411340 Product Usage: Intended for the fixation of f
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 Left 125 11 mm x 320 mm, Item Number 814411320 Product Usage: Intended for the fixation of f
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 Left 125 11 mm x 260 mm, Item Number 814411260 Product Usage: Intended for the fixation of f
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 Left 125 9 mm x 460 mm, Item Number 814409460 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 Left 125 9 mm x 440 mm, Item Number 814409440 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 Left 125 9 mm x 320 mm, Item Number 814409320 Product Usage: Intended for the fixation of fr
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 Left 125 9 mm x 300 mm, Item Number 814409300 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 Left 125 9 mm x 260 mm, Item Number 814409260 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 13 mm x 440 mm, Item Number 814313440 Product Usage: Intended for the fixation
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 400 mm, Item Number 814313400 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 13 mm x 360 mm, Item Number 814313360 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 300 mm, Item Number 814313300 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.