Stryker recalls Gamma4 Right Long Nail (catalog 84250320S) due to being manufactured with left nail geometry. This could cause improper function in surgical procedures.
Investigation confirmed that the GAMMA4 Right Long Nail was manufactured with the geometry of a left nail.
Stryker is recalling a specific Gamma4 surgical nail component because it was made with the geometry of a left nail instead of a right one. This could lead to improper use during surgery if the nail is installed incorrectly.
The Gamma4 Right Long Nail was manufactured with the geometry of a left nail. This means it may not fit correctly in the surgical system, potentially causing improper function during procedures. However, the risk is not immediate or life-threatening under normal use conditions.
Surgical teams using the Gamma4 System with this specific nail component are affected. Surgeons and surgical staff who have this model in their inventory or use it in procedures are most at risk.
Check for the catalog number 84250320S on the nail packaging or label. The product is part of the Gamma4 System and was sold with lot number K1BC9B7.
Look for the catalog number 84250320S on the nail packaging or label.
The Gamma4 Right Long Nail was manufactured with the geometry of a left nail instead of a right one, which could cause improper function during surgery.
This is a manufacturing error that could lead to improper function but does not pose an immediate risk of injury under normal use conditions.
Check for the catalog number 84250320S on the nail packaging or label. The product was sold with lot number K1BC9B7.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1914-2025 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1914-2025 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.
