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 surgery because the blister pack may not seal properly, risking contamination during procedures. This affects implants sold with specific catalog and lot numbers.

Why it’s dangerous

The blister pack's seal might be compromised, which could lead to contamination of the surgical implant. This affects sterility during procedures but does not cause immediate injury.

Who’s affected

Surgery patients and medical professionals using Stryker's locking screws for bone fixation. The risk is low as the hazard is related to packaging integrity rather than direct harm.

How to tell if you have this one

Check for catalog number 18965030S and lot numbers K0207B0, K02C1A8, K02C1A9, or K0302E4 on the packaging. These screws are used in bone surgery procedures.

Brand
Stryker
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for catalog number 18965030S and lot numbers K0207B0, K02C1A8, K02C1A9, or K0302E4 on the packaging.

✎ GovInfoNow

Questions people ask

Why is this screw being recalled?

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

What should I do if I have this product?

Check the catalog number and lot numbers on the packaging. If affected, contact Stryker for guidance.

Is this a safety hazard?

This is a sterility risk during surgery, not a direct safety hazard for the user.

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-2381-2020 — Stryker Stryker

Hello,

I own a Stryker that is covered by recall Z-2381-2020 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-2381-2020 (May 7, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2381-2020 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 ¿5x30 mm Catalog Number: 18965030S - Product Usage: Stryker implants are

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