Stryker recalls End Cap, Std, Ti Gamma3 (Catalog 30051100S) due to potential blister pack seal compromise affecting sterility. This single-use medical device may not be sterile if the blister pack is damaged.
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Stryker is recalling a specific bone fixation device because the blister pack that holds it might not seal properly, risking contamination. This is serious because medical implants are single-use and must be sterile to avoid infection.
The blister pack that contains the device may become compromised, meaning the device might not be sterile when used. Since this is a single-use medical implant, contamination could lead to serious infections or complications during surgery.
Patients who received this specific bone fixation device from Stryker. Medical professionals using the device for surgeries are most at risk.
Check for the catalog number 30051100S on the product label. This device is used for bone fixation and is part of Stryker's single-use implant line.
Immediately stop using the device if you have it, as it may not be sterile.
No, the device may not be sterile due to potential blister pack seal issues, so it should not be used.
Look for the catalog number 30051100S on the product label.
Stop using it immediately and contact Stryker for further instructions.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2387-2020 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2387-2020 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.
