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
April 26, 2017FDAvarious polyethylene implants Hips Active Articulation ArComXL Bearings Active Articu…Z-1860-2017
April 26, 2017FDAvarious polyethylene implants Knees Revision Tibial Tray Systems Oxford Partial Knee …Z-1861-2017
April 26, 2017FDAvarious polyethylene implants BIO PLUG 10MM Product Usage: Non-weight bearing a…Z-1858-2017
April 26, 2017FDAvarious polyethylene implants Sports Med Repicci II Tibial Components Product Usage…Z-1863-2017
April 19, 2017FDAMEDTECH ROSA Spine 1.0.2 The device is intended for the spatial positioning and orientat…Z-1755-2017
March 29, 2017FDAOrthosize Templating Version 1.2.6 Echo Bi-Metric Hip Stem Digital Templates. For preope…Z-1495-2017
February 22, 2017FDAVanguard Total Knee, PUNCH THRU TRL PLATES, 63 MM Item No: 32-487261, 67 MM Item No: 32-4…Z-1219-2017
February 22, 2017FDAComprehensive Reverse Shoulder System Humeral Tray Model 115340Z-1103-2017
February 8, 2017FDAVanguard Total Knee System Vanguard Open Box Femoral Components Item Number: 183100 …Z-1115-2017
February 8, 2017FDAOrthopedic Salvage System (OSS) 9cm prosthesis, knee, femorotibial, constrained, cemente…Z-1114-2017
January 25, 2017FDARingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall +3mm Liners Siz…Z-1024-2017
January 25, 2017FDAActive Articulation ArComXL Polyethylene Bearings Active Articulation ArComXL Bearings i…Z-1025-2017
January 18, 2017FDAOxford Fixed Lateral Bearing Size F Right, Part Number 154375 Lot 744260, Sterile, The pr…Z-0956-2017
October 26, 2016FDAVanguard Distal Femoral Augment 75 X 5 RL/LM Product Usage:  Painful and disabled kn…Z-0111-2017
March 16, 2016FDAM/L Taper Hip Prosthesis (Item: 00-7711-012-20, Lot: 62937093Z-1046-2016
March 2, 2016FDANexGen Knee CR Porous FEM NexGen Knee CR Precoat FEM prosthesis, knee, patellofemorotib…Z-0833-2016
March 2, 2016FDAVERSYS 6 INCH BEADED FC 1 VERSYS 6 INCH BEADED FC S VERSYS 8 INCH BEADED FC 1 VERSYS 8…Z-0849-2016
March 2, 2016FDANexGen LPS-FLEX Option Femoral NexGen LPS-FLEX Precoat Femoral prosthesis, knee, patell…Z-0832-2016
March 2, 2016FDANexGen LPS Flex Option Femoral NexGen LPS Flex Precoat Femoral prosthesis, knee, patell…Z-0841-2016
March 2, 2016FDACPT 12/14 COCR prosthesis, hip, semi-constrained, metal/polymer, porous uncemented vari…Z-0844-2016
March 2, 2016FDANexGen Knee CR Option Fem NexGen Knee CR Porous Fem NexGen Knee CR Precoat Fem NexGen …Z-0835-2016
March 2, 2016FDACR Flex GSF Precoat Fem Natural Knee GSF NP Flex Natural Knee GSF POR Flex Natural Kne…Z-0838-2016

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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