Every recall we track for Uromedica Inc. — 2 in all — plus the complaints and injury reports the public filed about them.
Uromedica recalls specific implantation instrument sets (REF 750041) due to potential damage to ProACT devices during surgery. Affected units have lot numbers UM00794 or UM00817.
Uromedica recalls ProACT Implantation Instrument Set (Model 750041, Lot UM00650) due to potential U-channel sheath damage to implant devices during use. Affected units may cause device damage when passed through sheaths.
