Reported Oct 26, 2022 · Ongoing
SPEED 9X10X10mm Continuous Compression Implant, Product No. SE-0910
Synthes (USA) Products LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Synthes (USA) Products LLC · 1301 Goshen Pkwy · West Chester, PA · 19380-5986
Is this the product you have?
- SPEED 9X10X10mm Continuous Compression Implant, Product No. SE-0910
- Lot codes and dates
- UDI-DI (GTIN)00810633020111 Lot/Expiry MSE210240 7/1/2027
- Amount recalled
- 96
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
- Nationwide
Why it was recalled
The subject products are being recalled because they contain the incorrect size drill guide and will not prepare the bone correctly for the size of the implant included in the sterile kit. If the incorrect drill guide is used, there is potential for bone damage due to incorrectly placed drill holes for the implant included in the kit.
This product could cause temporary or reversible health problems — stop using it.
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