Stryker Tibial Tray Recall: Oversized Lock Risk

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Recalling firmWright Medical Technology, Inc.1023 Cherry Rd, N/A · Memphis, TN 38117-5423

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Stryker is recalling left plasma spray tibial trays with an oversized lock detail that could cause improper fit during surgery. This recall affects specific surgical implants used with 18mm stem bases.

Why it’s dangerous

The tibial tray lock detail is larger than it should be, which could lead to improper alignment during surgery. This might cause the implant to shift or not function correctly in the patient's bone.

Who’s affected

Surgical teams using the specific Stryker INBONE Tibial Tray model (REF 200252904, Size 4) are affected. Orthopedic surgeons and their surgical teams face the highest risk.

How to tell if you have this one

Check for the model name 'Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti' with the reference number 200252904 and size 4. The product was sold with a specific lot code.

Brand
Stryker
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Identify the model number, reference number, and size to confirm if your item is affected.

✎ GovInfoNow

Questions people ask

Is this recall dangerous?

The recall states the lock detail is oversized, which could cause improper fit during surgery, but the remedy is not specified so the risk level is low.

How do I know if my product is affected?

Check for the model name 'Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti' with reference number 200252904 and size 4.

What should I do if I have this product?

The recall does not specify a remedy, so no action is required at this time.

Take action

Contact Stryker

We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0140-2023 — Stryker Stryker

Hello,

I own a Stryker that is covered by recall Z-0140-2023 from Stryker.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0140-2023 (September 30, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0140-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Wright Medical Technology, Inc. recalls Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 18mm Stem Base, REF 200252904, Size 4

Lower-risk recall