Reported Oct 26, 2022 · Ongoing
DePuy Synthes Hammertoe Continuous Compression Implants, Product No. 46.239.001
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?
- DePuy Synthes Hammertoe Continuous Compression Implants, Product No. 46.239.001
- Lot codes and dates
- UDI-DI (GTIN)00810633022047 Lot/Expiry MHC200114 2/9/2026 MHC220117 3/2/2027
- Amount recalled
- 196
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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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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