Stry: Precision Thin Blades May Not Fit Handpieces
Stryker recalls Precision Thin blades (REF 2296-003-155) that may not securely fit handpieces due to measurement issues. Affected units include specific lot numbers and GTIN.
Lower-risk recall
Precision Thin blade attachments have a potential to be out of measurement specifications, preventing them from securely fitting into the compatible handpiece.
Contact the company
What happened, in plain English
Stryker is recalling Precision Thin blades that might not fit properly into their handpieces because of measurement problems. This could lead to improper use or damage during dental procedures. Read more at govinfonow.com/recall/53140-stry-precision-thin-blades-may-not-fit-handpieces.
Source Summary by GovInfoNow · govinfonow.com/recall/53140-stry-precision-thin-blades-may-not-fit-handpieces · Updated September 23, 2026 · FDA enforcement record: FDA #Z-1139-2025
Cite this page
“Stry: Precision Thin Blades May Not Fit Handpieces.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/53140-stry-precision-thin-blades-may-not-fit-handpieces. Based on FDA recall #Z-1139-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1139-2025%22&limit=1).
Why it’s dangerous
The blades may not fit securely into the handpieces due to measurement issues. This could cause improper function during dental procedures, potentially leading to equipment damage or ineffective treatment.
Who’s affected
Dentists and dental clinics using the recalled Precision Thin blades (Catalog Number REF 2296-003-155) are most at risk. Patients using these blades during dental procedures may also be affected.
How to tell if you have this one
Check for the Catalog Number REF 2296-003-155 on the blade packaging. The product was sold with GTIN 04546540466549 and Lot Number 23070017.
- Brand
Stryker- Product
stryker Precision Thin, Catalog Number REF 2296-003-155; Micro Oscillating and Sagittal Blades- Category
Medical device
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- Distribution
Worldwide distribution.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-1138-2025 | stryker Precision Thin, Catalog Number REF 2296-003-108; Micro Oscillating and Sagittal Blades; GTIN 04546540046482, Lot Number 22298017 | 622 units |
| Z-1139-2025 | stryker Precision Thin, Catalog Number REF 2296-003-155; Micro Oscillating and Sagittal Blades; GTIN 04546540466549, Lot Number 23070017 | 238 units |
What to do — step by step
Check Blade Fit
Ensure the blade securely fits into the handpiece before use. If it doesn't fit properly, stop using it.
How this recall unfolded
Recall timeline
FDA published this recall 42 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-1139-2025 (January 8, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1139-2025 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.