Stryker recalls QuickFlap sterile procedure packs that may have compromised packaging after 3 years, risking infection. Affected users should contact Stryker for details.
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Stryker recalls QuickFlap sterile procedure packs that could have compromised packaging after three years, potentially leading to infection risks. This affects medical devices used in surgeries for skull fractures.
After three years, the sterile packaging might become compromised, increasing the risk of infection during surgery. This is a potential issue for medical devices used in procedures involving skull fractures.
Adults and adolescents aged 12 and older who use Stryker QuickFlap packs for skull fracture repairs. Those with the specific part number 12-01521S are most at risk.
Check for the part number 12-01521S on the packaging. The product is a sterile procedure pack for skull fracture repairs in adults and adolescents aged 12 and older.
Reach out to Stryker directly for specific instructions on handling the recalled product.
The recall states there is a potential for the packaging to become compromised after three years, so it is not recommended for use beyond that time.
Contact Stryker directly for specific instructions on handling the recalled product.
The recall indicates a potential risk after three years, so it is not recommended for use beyond that time.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2899-2018 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2899-2018 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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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.
