Zimmer Biomet, Inc.: 222 recalls on record

Recalls filed with 1 agency: FDA (222).

First recall on record: March 2, 2016. Most recent: December 30, 2020.

Risk classification: Class I: 2 · Class II: 220

Most recent recalls

DateAgencyProduct
February 21, 2018FDAG7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use in hip arthroplasty cas…Z-0626-2018
February 14, 2018FDAM/DN Intramedullary Fixation Humeral Guide Wire - Bullet Tip 2.4 mm Diameter 70 cm Length…Z-0548-2018
February 14, 2018FDAM/DN Intramedullary Fixation Humeral Guide Wire - Smooth 2.4 mm Diameter 70 cm Length Sin…Z-0547-2018
February 7, 2018FDAAffixus Hip Fracture Nail, RH 130 DEG 11MM X 440MMZ-0471-2018
February 7, 2018FDAAffixus Hip Fracture Nail, RH 125 DEG 11MM X 440MMZ-0450-2018
February 7, 2018FDAAffixus Hip Fracture Nail, RH 130 DEG 9MM X 320MMZ-0478-2018
February 7, 2018FDAAffixus Hip Fracture Nail, 125 DEG 11MM X 180MMZ-0420-2018
February 7, 2018FDAAffixus Hip Fracture Nail, LH 125 DEG 11MM X 360MMZ-0425-2018
February 7, 2018FDAAffixus Hip Fracture Nail, 130 DEG 9MM X 180MMZ-0423-2018
February 7, 2018FDAAffixus Hip Fracture Nail, LH 130 DEG 11MM X 340MMZ-0434-2018
February 7, 2018FDAAffixus Hip Fracture Nail, LH 130 DEG 9MM X 400MMZ-0445-2018
February 7, 2018FDAAffixus Hip Fracture Nail, RH 130 DEG 9MM X 340MMZ-0479-2018
January 10, 2018FDACER OPTION TYPE 1 TPR SLEVE -6, model # 650-1064Z-0301-2018
January 10, 2018FDARED SEXP DSTL FEM 19CM RT ASSY, model # CP111817Z-0304-2018
December 6, 2017FDAROSA Surgical Device 2.5.8Z-0178-2018
November 29, 2017FDAROSA BRAIN 3.0.0Z-0116-2018
November 29, 2017FDAROSA Brain 3.0.0 Usage: The device is intended for the spatial positioning and orient…Z-0167-2018
November 29, 2017FDAROSA Surgical Device 2.5.8, a computer-controlled electromechanical arm to guide standard…Z-0160-2018
November 29, 2017FDAROSA Surgical Device 2.5.8 It is intended to be used in the operating room for the s…Z-0161-2018
November 22, 2017FDAROSA Surgical Device 2.5.8. It is intended to be used in the operating room for the s…Z-0102-2018
November 22, 2017FDAROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled electromechani…Z-0099-2018
October 4, 2017FDAECT Internal Fracture Fixation Drill 3.5 mm Diameter (.138 Inch), Item Number/EDI 0023180…Z-3172-2017
October 4, 2017FDADrill Bit Quick-Connect 1.1 mm Diameter 60 mm Length, Item Number/EDI 00480606011, Nonst…Z-3153-2017
October 4, 2017FDAECT Internal Fracture Fixation Quick-Connect Drill 2.7 mm Diameter 10 cm Length, Item Num…Z-3186-2017
October 4, 2017FDADrill Bit Jacobs Chuck 2.0 mm Diameter 85 mm Length, Item Number/EDI 00480508520, Nonster…Z-3190-2017

Questions about this company

How many recalls does Zimmer Biomet, Inc. have?
Recalert has 222 U.S. recalls on record for Zimmer Biomet, Inc., published between March 2, 2016 and December 30, 2020.
Which agencies have handled Zimmer Biomet, Inc. recalls?
Zimmer Biomet, Inc. appears as the recalling firm in recalls from: FDA (222).

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