Stryker recalls Precision Thin blades (REF 2296-003-108) that may not securely fit handpieces, risking improper use. Affected units include specific lot numbers and GTIN.
Precision Thin blade attachments have a potential to be out of measurement specifications, preventing them from securely fitting into the compatible handpiece.
Stryker is recalling Precision Thin blades that might not fit securely into their handpieces. This could lead to improper use if the blades don't attach correctly.
The blades may be out of measurement specifications, causing them to not fit securely into the handpiece. This could lead to improper use during dental procedures.
Stryker Precision Thin blade users who purchased the recalled model (REF 2296-003-108) are affected. Dental professionals using these blades are most at risk.
Check for the catalog number REF 2296-003-108 on the blade packaging or label. The product also has a GTIN of 04546540046482 and lot number 22298017.
Ensure the blade securely attaches to the handpiece before use. If it doesn't fit properly, stop using it.
The recall does not specify a return process, so no action is required beyond checking the fit.
The catalog number is REF 2296-003-108.
The blades may not fit securely, which could lead to improper use during dental procedures.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1138-2025 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1138-2025 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.
