Stryker Locking Screw Recall: Blister Pack Sterility Risk

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Recalling firmStryker GmbHBohnackerweg 1 · Selzach, N/A

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Stryker is recalling certain locking screws used in bone implants because the blister packaging might not be sterile. This could lead to infections if the screws are used without proper sterility.

Why it’s dangerous

The blister pack may become compromised, meaning the screws could be contaminated. This risks infection during surgery if the screws are not sterile.

Who’s affected

Orthopedic surgeons and medical professionals who use these screws for bone fixation. Patients receiving these implants are at risk if the screws are not sterile.

How to tell if you have this one

Check for catalog number 18965037S and lot numbers K029C38 through K031B66. These screws are used in bone implants and sold by Stryker.

Brand
Stryker
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Verify the catalog number and lot numbers to confirm if your screws are affected.

✎ GovInfoNow

Questions people ask

Why is this recall happening?

The blister pack may be compromised, risking contamination and infection during surgery.

What should I do if I have these screws?

Check the catalog number and lot numbers to see if they are affected. Contact Stryker for further instructions.

Are these screws safe to use?

The recall indicates potential sterility issues, so affected units should not be used until resolved.

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-2383-2020 — Stryker Stryker

Hello,

I own a Stryker that is covered by recall Z-2383-2020 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-2383-2020 (May 7, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2383-2020 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.

Stryker GmbH recalls Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x37,5 mm Catalog Number: 18965037S - Product Usage: Stryker implants

Lower-risk recall