Stryker, T2 K-Wire, 3.2x400mm, Recon Product Usage: Intended for the temporary stabilization of bone segments or fragments.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Catalog number 1806-3030S; All lots distributed before 10 Nov 2015 with non-expired 5 year shelf life
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Stryker Howmedica Osteonics Corp.
- Reason for Recall:
- During a review of the packaging, it was determined that the seal integrity of the pouch may be decreased.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Stryker, T2 K-Wire, 3.2x400mm, Recon Product Usage: Intended for the temporary stabilization of bone segments or fragments.
Product Codes/Lot Numbers:
Catalog number 1806-3030S; All lots distributed before 10 Nov 2015 with non-expired 5 year shelf life
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0883-2016
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Stryker Howmedica Osteonics
A review of packaging revealed the seal integrity of the pouch may be compromised. More specifically, there is a potential that the sterile pouch is not sealed at one end due to a manufacturing error.