Recall Register

Food, drugs, devices › Firms

Zimmer Trabecular Metal Technology, Inc.

FDA recalling firm · 5 enforcement events · 11 product records · 2014–2019 · NJ

Zimmer Trabecular Metal Technology, Inc. has 5 FDA enforcement events on this register (11 product records) between 2014 and 2019: 5 device; the busiest year was 2016 with 2.

0% of its events are Class I; the most common class is Class II (4). 0 events are listed as ongoing; the recalling firm's address is in NJ.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
1 Feb 2019NexGenTrabecular Metal Tibial Half Block Augment, Right Lateral/Left Medial, Size 4 5MM Thickness W/Screws Item Number: 00544800426 Product Usage: The Trabecular Metal Tibial Cone Augments are intended for use where severe degeneration, trauma, or other pathology of the knee joint indicates total knee arthroplasty.…DeviceClass II2Terminated
7 Jul 2016The TM Ardis Interbody System implant is a convex, straight TLIF or PLIF device for interbody fusion of the anterior column of the spine. TM Ardis is designed for fusing the adjacent bony surfaces and may be used to replace a disc at one or two contiguous levels in L2-S1. The superior and inferior surfaces of the…DeviceClass III1Terminated
15 Apr 2016POROUS PATELLA 32MM X 10MM - 00587806532 POROUS PATELLA 35MM X 10MM- 00587806535 POROUS PATELLA 38MM X 10MM - 00587806538 POROUS PATELLA 41MM X 10MM - 00587806541DeviceClass II6Terminated
4 Feb 2015NexGen TRABECULAR METAL FEMORAL AUGMENT BLOCK DISTAL ONLY, 20 MM Augment, Size D, Sterile, Rx Only. Product Usage: Intended for use where severe degeneration, trauma, or other pathology of the knee joint indicates total knee arthroplasty. When used with the NexGen Complete Knee Solution-Rotating Hinge Knee (RHK)…DeviceClass II1Terminated
2 Dec 2014NexGen Complete Knee Solution Monoblock Tibial Provisional / Drill Guide Tibial Size 5 Femoral Size Green / CH Zimmer U.K. Ltd., SN3 4FP, UK Zimmer Trabecular Metal Technology, Inc 10 Pomeroy Road, Parsippany, NJ 07054 USADeviceClass II1Terminated

By type and class

Device5
Class II4
Class III1

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

14
16
18
20
22
24
26
Enforcement events for Zimmer Trabecular Metal Technology, Inc. by year initiated.

Questions and answers

How many FDA recalls has Zimmer Trabecular Metal Technology, Inc. had?

5 enforcement events (11 product records) on this register, 2014–2019: 5 device.

Are any Zimmer Trabecular Metal Technology, Inc. recalls ongoing?

0 events are listed as ongoing in the current openFDA export.

What class are Zimmer Trabecular Metal Technology, Inc. recalls?

4 Class II, 1 Class III. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.