Trident PSL Acetabular Shell recallZ-1261-2007 · Stryker Howmedica Osteonics Corp. · initiated Mar 13, 2006
Terminated All recalls posted in September 2007
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 Stryker Howmedica Osteonics Corp. 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
Dimensional anomaly
FDA root cause category: Other
What the company is doing
Recall Notification letters were sent on March 13, 2006 to all hospitals, branches/agencies via Federal Express.
Recall details
- Recall number
- Z-1261-2007
- Recall class
- Not yet classified by the FDA
- Status
- Terminated
- Initiated by the company
- Mar 13, 2006
- Posted by the FDA
- Sep 26, 2007
- Recalling firm
- Stryker Howmedica Osteonics Corp.
- Quantity
- 1,220 units
- Product code
- MEH
- FDA submissions
- K983382
- Distribution
- Worldwide -USA, Romania, Chile and Brazil.
Product description
Trident PSL Acetabular Shell;Arc Deposited;Hydroxylapatite Coated;Cluster Screw Holes;Howmedica Osteonics Corp., 325 Corporate DriveMahway, NJ 07430
Code information (models, lots, serial numbers)
Show the full code information (3k characters)
Catalog number/ lot code: 540-11-56F 36906101 540-11-58G 37048901 540-11-58G 37122001 542-11-46D 34977701 542-11-46D 35105901 542-11-46D 35382701 542-11-46D 35483101 542-11-46D 35525001 542-11-46D 35584201 542-11-46D 37497001 542-11-46D 37830601 542-11-46D 37884701 542-11-46D 38034101 542-11-46D 38124501 542-11-48D 35028401 542-11-48D 35332701 542-11-48D 35406002 542-11-48D 35406003 542-11-48D 35687701 542-11-48D 35726401 542-11-48D 35834801 542-11-48D 37790101 542-11-48D 37891501 542-11-48D 38025001 542-11-48D 38025002 542-11-48D 38160501 542-11-50E 35032701 542-11-50E 35207301 542-11-50E 35385903 542-11-50E 35428901 542-11-50E 35428903 542-11-50E 35481501 542-11-50E 35481502 542-11-50E 35481502 542-11-50E 35515802 542-11-50E 35827902 542-11-50E 36966303 542-11-50E 37344301 542-11-50E 37515302 542-11-50E 37695201 542-11-50E 37888201 542-11-50E 37920201 542-11-50E 38245801 542-11-50E 38274303 542-11-52E 32886803 542-11-52E 35018402 542-11-52E 35018403 542-11-52E 35018404 542-11-52E 35085001 542-11-52E 35199201 542-11-52E 35199202 542-11-52E 35199204 542-11-52E 35325401 542-11-52E 35325403 542-11-52E 35373402 542-11-52E 35373403 542-11-52E 35419904 542-11-52E 35726002 542-11-52E 35866302 542-11-52E 35866304 542-11-52E 37057001 542-11-52E 37096702 542-11-52E 37368002 542-11-52E 37886202 542-11-52E 37886204 542-11-52E 37886206 542-11-52E 37925602 542-11-52E 37995901 542-11-52E 37995902 542-11-54F 35091602 542-11-54F 35186502 542-11-54F 35732703 542-11-54F 35868801 542-11-54F 35965101 542-11-54F 37443401 542-11-54F 37443403 542-11-54F 37789201 542-11-54F 37916502 542-11-54F 38095601 542-11-54F 38223203 542-11-56F 35081001 542-11-56F 35225301 542-11-56F 35225302 542-11-56F 35225303 542-11-56F 35290801 542-11-56F 35335101 542-11-56F 35524501 542-11-56F 35535102 542-11-56F 35831001 542-11-56F 36330001 542-11-56F 36542101 542-11-56F 36542102 542-11-56F 36768001 542-11-56F 36907201 542-11-56F 37050902 542-11-56F 37461501 542-11-56F 37743301 542-11-56F 38099001 542-11-58G 35638002 542-11-58G 35959701 542-11-58G 35959702 542-11-58G 36052801 542-11-58G 36137301 542-11-58G 36195501 542-11-58G 36195502 542-11-58G 36332802 542-11-58G 36372301 542-11-58G 36412601 542-11-58G 36430601 542-11-58G 36489601 542-11-58G 36489602 542-11-58G 36553001 542-11-58G 36583801 542-11-58G 36633201 542-11-58G 36758901 542-11-58G 36758902 542-11-58G 36898201 542-11-58G 37049101 542-11-58G 37049102 542-11-58G 37049103 542-11-58G 37122401 542-11-58G 37122402 542-11-58G 37122403 542-11-58G 37173201 542-11-58G 37242901 542-11-58G 37242902 542-11-58G 37279901 542-11-58G 37332301 542-11-58G 37500801 542-11-58G 37500801 542-11-58G 37500803 542-11-58G 37826804 542-11-60G 34806101 542-11-60G 34907101 542-11-60G 35666901 542-11-60G 35946101 542-11-60G 36002201 542-11-60G 36406701 542-11-60G 36435401 542-11-60G 36765101 542-11-60G 37119701 542-11-60G 37119702 542-11-60G 37273901 542-11-60G 37402101 542-11-62G 37358901 542-11-62H 34930801 542-11-62H 35272101 542-11-62H 35508901 542-11-62H 36270401 542-11-62H 36842101 542-11-64H 36406301 542-11-64H 37082601 542-11-64H 37358801 542-11-64H 37859901
Other devices under the same FDA submission
9 devices cleared under K983382 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.
- Trident 621-00-28EHowmedica Osteonics Corp. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- Trident 621-00-28GHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
- Trident 621-00-28IHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
- Trident 621-10-26EHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
- Trident 621-10-26DHowmedica Osteonics Corp. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Trident 621-10-26FHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
- Trident 621-10-28EHowmedica Osteonics Corp. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Trident 621-10-28FHowmedica Osteonics Corp. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Trident 621-10-28GHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
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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