Home / Recalls / Medical Devices
Synthes (USA) Products LLC recalls DePuy Synthes Hammertoe Continuous Compression Implants, Product No. 46.239.001
Recalled October 26, 2022 · FDA recall Z-0101-2023 · Synthes (USA) Products
Hazard
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. · FDA Class II
Units
196
Sold at
US Nationwide distribution.
Description
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.
Product
DePuy Synthes Hammertoe Continuous Compression Implants, Product No. 46.239.001
Manufacturer(s)
Synthes (USA) Products LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →