Stryker recalls a specific locking screw implant due to potential blister pack compromise affecting sterility. This could lead to infection risks during surgery. Affected units have catalog number 18915055S.
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Stryker is recalling a specific type of bone screw implant because the blister pack might not stay sealed properly. This could mean the screw isn't sterile when used in surgery, increasing infection risks for patients.
The blister pack that holds the screw may not stay sealed correctly. This could allow contamination, meaning the screw might not be sterile when used in surgery. If the screw isn't sterile, it could cause infections in patients.
Stryker implant users who purchased the specific locking screw with catalog number 18915055S. Patients undergoing surgery with this implant are at risk of infection if the screw isn't properly sterile.
Check for the catalog number 18915055S on the blister pack. This screw is used for bone fixation in surgeries and was produced in lot K01CF9F.
Look for the catalog number 18915055S on the blister pack to confirm if this specific screw is affected.
The blister pack may not stay sealed properly, which could compromise sterility and lead to infection risks during surgery.
The recall is due to potential sterility issues, not immediate danger. Proper use with a sterile process should prevent infection risks.
Check for the catalog number 18915055S on the blister pack. This screw is used for bone fixation in surgeries and was produced in lot K01CF9F.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2379-2020 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2379-2020 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.
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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.
