Reported Jun 24, 2020 · Terminated

Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x50 mm Catalog Number: 18965050S - Product Usage: Stryker implants are…

Stryker GmbH

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Stryker GmbH · Bohnackerweg 1 · Selzach · N/A

Is this the product you have?

  • Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x50
  • mm Catalog Number18965050S -
  • Product UsageStryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones
Lot codes and dates
  • Lot Number
    • K030F1E
    • K033442
Amount recalled
OUS 121

This recall covers 15 products

The agency filed one notice per product. You are reading one of them; the other 14 are below.

2 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Seal integrity of the blister pack may be compromised and sterility cannot be assured

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Sep 21, 2023 · Data as of Sep 19, 6:50 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.