Stryker Locking Screw Recall: Blister Pack Sterility Risk

Take action

Contact the company & request your remedy

Recalling firmStryker GmbHBohnackerweg 1 · Selzach, N/A

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Stryker is recalling a specific locking screw used in bone implants because the blister pack might not keep it sterile. If the pack isn't sealed properly, the screw could cause infection during surgery.

Why it’s dangerous

The blister pack may not seal properly, which could allow contamination. This means the screw might not be sterile when used in surgery, increasing infection risk.

Who’s affected

Surgery patients receiving this specific screw for bone fixation. Surgeons and medical staff using the product are most at risk.

How to tell if you have this one

Check for catalog number 17965035S on the packaging. The product is used for bone implants and was manufactured with lot number K0386FB.

Brand
Stryker
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for catalog number 17965035S on the packaging or label.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall states the blister pack may not seal properly, so sterility cannot be assured. This could lead to infection during surgery.

How can I tell if I have the recalled product?

Check for catalog number 17965035S on the packaging. The product is used for bone implants and was manufactured with lot number K0386FB.

What should I do if I have this product?

The recall does not specify a remedy, so contact Stryker directly for guidance.

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-2373-2020 — Stryker Stryker

Hello,

I own a Stryker that is covered by recall Z-2373-2020 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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-2373-2020 (May 7, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2373-2020 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 S2 05x35 mm Catalog Number: 17965035S - Product Usage: Stryker implants are

Lower-risk recall