Zimmer ZMR Hip System femoral body, revision, nitrided… recallZ-1476-06 · Zimmer Inc. · initiated Aug 2, 2006

Terminated All recalls posted in August 2006

Is my device affected?

Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
If yours is listed, follow the instructions from Zimmer Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

Lack of assurance of proper metal fatigue strength due to a metal grain structure anomaly.

FDA root cause category: Other

What the company is doing

Consignees were notified via letter dated 8/2/06 to cease use of and to return the products. Zimmer distributors were to examine stock and return product on hand.

Recall details

Recall number: Z-1476-06
Recall class: Not yet classified by the FDA
Status: Terminated
Initiated by the company: Aug 2, 2006
Posted by the FDA: Aug 31, 2006
Recalling firm: Zimmer Inc.
Quantity: 181 of all devices
Product code: LPH
FDA submissions: K994286
Distribution: Worldwide, including USA, Australia, China, Denmark, Japan, Jordan, Latin Ameria, Russia, Singapore and Switzerland.

Product description

Zimmer ZMR Hip System femoral body, revision, nitrided, porous, 12/14 neck taper, extended, 46 mm neck offset, spout body, size D, 35 mm build-up, tivanium TI-6AL-4V alloy, sterile; REF. 9990-20-46 (Cat. no. 00999002046).

Code information (models, lots, serial numbers)

Lot 60465192.

Other devices under the same FDA submission

3 devices cleared under K994286 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.

ZMR® 9993-18-35
Zimmer, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
1 report
ZMR® 9996-17-45
Zimmer, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented
1 report
ZMR® 9996-19-35
Zimmer, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
1 report

Other products in the same recall event

The FDA groups related products into one recall event (event 35943).

Z-1471-06 · Terminated
Zimmer Trabecular metal primary hip prosthesis femoral stem, press-fit, collarless, 12/14 neck taper - standard body -extended neck offset, size 14, 149 mm stem length, sterile, ti…
Z-1472-06 · Terminated
Zimmer Trabecular metal primary hip prosthesis femoral stem, press-fit, collarless, 12/14 neck taper - standard body -extended neck offset, size 15, 160 mm stem length, sterile, ti…
Z-1473-06 · Terminated
Zimmer Trabecular metal primary hip prosthesis femoral stem, press-fit, collarless, 12/14 neck taper - standard body -standard neck offset, size 16, 171 mm stem length, sterile, ti…
Z-1477-06 · Terminated
Zimmer ZMR Hip System femoral body, revision, nitrided, porous, 12/14 neck taper, extended, 46 mm neck offset, cone body, size C, 55 mm build-up, tivanium TI-6AL-4V alloy, sterile;…
Z-1478-06 · Terminated
Zimmer ZMR Hip System femoral body, revision, nitrided, porous, 12/14 neck taper, standard, 40 mm neck offset, cone body, size C, 35 mm build-up, tivanium TI-6AL-4V alloy, sterile;…
Z-1479-06 · Terminated
Zimmer ZMR Hip System femoral body, revision, nitrided, porous, 12/14 neck taper, standard, 40 mm neck offset, cone body, size C, 45 mm build-up, tivanium TI-6AL-4V alloy, sterile;…
Z-1480-06 · Terminated
Zimmer ZMR Hip System femoral body, revision, nitrided, porous, 12/14 neck taper, standard, 40 mm neck offset, cone body, size F, 35 mm build-up, tivanium TI-6AL-4V alloy, sterile;…

Sources and updates

Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
Page last rebuilt: Oct 18, 2026. Text above is shown as published by the FDA.

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