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Zimmer Trabecular Metal Technology Recalls
11 recalls on record · December 31, 2014 to March 20, 2019 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
March 20, 2019Medical DevicesFDA
Zimmer Trabecular Metal Technology, Inc. recalls NexGenTrabecular Metal Tibial Half Block Augment, Left Lateral/Right Medial, Size 4 5MM Thickness W/Screws Item Number
Hazard: Potentially comingled, resulting in the product in the box potentially not matching the product on the label
March 20, 2019Medical DevicesFDA
Zimmer Trabecular Metal Technology, Inc. recalls NexGenTrabecular Metal Tibial Half Block Augment, Right Lateral/Left Medial, Size 4 5MM Thickness W/Screws Item Number
Hazard: Potentially comingled, resulting in the product in the box potentially not matching the product on the label
May 10, 2017Medical DevicesFDA
Zimmer Trabecular Metal Technology, Inc. recalls The TM Ardis Interbody System implant is a convex, straight TLIF or PLIF device for interbody fusion of the anterior col
Hazard: This field action is being initiated following the firm's discovery of a procedural error in the approval of literature resulting in the undo release of certain content. Information was disseminated to distributors and sales representatives during the 2016 National Sales Meeting held February 17-21, 2016.
June 22, 2016Medical DevicesFDA
Zimmer Trabecular Metal Technology, Inc. recalls 00720504022 ACETAB.CUPW/SH,0DEG,22MMX40MM 00720504222 ACETAB.CUPW/SH,0DEG,22MMX42MM 00720504622 ACETAB.CUPW/SH,0DEG,
Hazard: Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.
June 22, 2016Medical DevicesFDA
Zimmer Trabecular Metal Technology, Inc. recalls REV. SHELL LINER 0D 28X48 00700504828 REV. SHELL LINER 10D 28X50 00701005028 REV. SHELL LINER 10D 28X52 007010052
Hazard: Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.
June 22, 2016Medical DevicesFDA
Zimmer Trabecular Metal Technology, Inc. recalls TM MONO TIB STR GRN SZ 5 - 00588606510 TM MONO TIB STR GRN SZ 5 12MM - 00588606512 TM MONO TIB STR GRN SZ 5 14MM - 005
Hazard: Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.
June 22, 2016Medical DevicesFDA
Zimmer Trabecular Metal Technology, Inc. recalls TM LPS TIB SZ 3 C/D, 10MM - 00588605310 TM LPS TIB SZ 3 C/D, 12MM - 00588605312 TM LPS TIB SZ 3 C/D, 14MM - 005886
Hazard: Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.
June 22, 2016Medical DevicesFDA
Zimmer Trabecular Metal Technology, Inc. recalls TM CR TIB SZ 3 C-H, 10MM- 00588604310 TM CR TIB SZ 3 C-H, 12 mm - 00588604312 TM CR TIB SZ 3 C-H, 14MM - 0058860
Hazard: Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.
June 22, 2016Medical DevicesFDA
Zimmer Trabecular Metal Technology, Inc. recalls POROUS PATELLA 32MM X 10MM - 00587806532 POROUS PATELLA 35MM X 10MM- 00587806535 POROUS PATELLA 38MM X 10MM - 005
Hazard: Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.
April 1, 2015Medical DevicesFDA
Zimmer Trabecular Metal Technology, Inc. recalls NexGen TRABECULAR METAL FEMORAL AUGMENT BLOCK DISTAL ONLY, 20 MM Augment, Size D, Sterile, Rx Only. Product Usage: I
Hazard: One unit of the 20 mm augments was mislabeled as 5 mm and it was subsequently distributed.
December 31, 2014Medical DevicesFDA
Zimmer Trabecular Metal Technology, Inc. recalls NexGen Complete Knee Solution Monoblock Tibial Provisional / Drill Guide Tibial Size 5 Femoral Size Green / CH Zimmer U
Hazard: During cleaning, two separate units of the NexGen Tibial Base plates did not fit with the Tibial Base Plate handle.