Reported Jun 24, 2020 · Terminated
Stryker End Cap T2 Tibia +10 mm Catalog Number: 18220010S - Product Usage: Stryker implants are single use devices…
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 End Cap T2 Tibia +10
- mm Catalog Number18220010S -
- Product UsageStryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones
- Lot codes and dates
- Lot Number
K020795K020796
- Lot Number
- Amount recalled
- 186 OUS
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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