Stryker recalls INFINITY Resect Guide for INBONE Talus, Size 4 (Model #33620254) due to incorrect color coding. This may cause confusion during surgical procedures. Affected units were sold with Lot #2039558 and GTIN 00889797006552.
The instrument is incorrectly color coded.
Stryker is recalling a specific surgical instrument (INFINITY Resect Guide for INBONE Talus, Size 4) because it has incorrect color coding. This could lead to confusion during surgery, potentially affecting patient safety.
The instrument has incorrect color coding, which could lead to confusion during surgical procedures. This might cause the wrong instrument to be used, potentially affecting the procedure's outcome. However, this is a labeling issue, not a physical hazard.
Surgical teams using the Stryker INFINITY Resect Guide for INBONE Talus, Size 4 (Model #33620254) are affected. The risk is low as this is a color coding issue, not a safety hazard.
Check for the model number 33620254 on the instrument. The product was sold with Lot #2039558 and GTIN 00889797006552. This instrument is non-sterile and used with the INFINITY Total Ankle System.
Look for the model number 33620254 on the instrument to confirm if it is affected.
The product is safe to use as long as the model number matches the recalled item. Incorrect color coding may cause confusion but does not pose a physical hazard.
The official recall does not specify a remedy, so no action is required beyond checking the model number.
Check for the model number 33620254, Lot #2039558, and GTIN 00889797006552 on the instrument.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1291-2022 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1291-2022 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.
