Stryker recalls specific lots of Infinity Resection Adjustment Blocks for ankle surgery due to missing internal screw that could affect joint alignment during procedures.
Stryker has identified an issue that impacts specific lots of Infinity" Resection Guide Adjustment Blocks. The parts within these three lots were found to have been missing an internal screw in the finished instrument assembly. The missing screw is used to lockout the Medial/Lateral adjustment on the INFINITY Resection Adjustment Guide.
Stryker is recalling three specific lots of Infinity Resection Adjustment Blocks used in ankle surgery because they may be missing an internal screw. This could cause improper joint alignment during surgery if the block is used without the screw.
The missing screw prevents proper locking of the Medial/Lateral adjustment on the block. Without this screw, the block may not stay securely in place during surgery, potentially causing improper joint alignment.
Surgery patients and medical professionals who use the recalled blocks for ankle arthroplasty procedures. Those with the specific lot numbers are most at risk.
Check the lot numbers: 2656950, 2762126, or 2796094. The product is used in ankle arthroplasty procedures and has a UDI/DI code of 00889797004008.
Identify if your block has lot numbers 2656950, 2762126, or 2796094.
The recalled blocks may be missing an internal screw that locks the Medial/Lateral adjustment, which could cause improper joint alignment during surgery.
The recall record does not specify a remedy, so contact Stryker directly for guidance.
Check the lot numbers: 2656950, 2762126, or 2796094. The product is used in ankle arthroplasty procedures and has a UDI/DI code of 00889797004008.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1477-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1477-2024 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.
