Encore Medical, LP
32 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Encore Medical, LP and translate it into plain English — free weekly digest, optional same-day alerts.
- 2023-09-27FDA-DeviceClass IIDJO Surgical: Empowr Knee, Universal Tibia Baseplate, 6R, REF: 352-02-106
Orthopedic device components were not subjected to final sterilization before shipment, which if implanted may lead to varying degrees of infection, which may require treatment, prolonged monitoring, and may lead to revision surgery
- 2023-04-19FDA-DeviceClass IIEMPOWR Porous Knee Patella Over Drill, REF: 802-05-104; EMPOWR Knee Patella Drill, REF: 802-05-108
Patella drills are marked with incorrect diameter size of 5.6mm, when they should be 5.4mm. Porous patella overdrills are marked with incorrect diameter size of 5.4 mm, when they should be 5.6 mm. If the incorrect drill is selected during surgery, there is risk of the implant loosening, implant not properly fitting, and/or fractured bone.
Get notified about new Encore Medical, LP recalls
Free weekly digest. We email when a new federal recall affects Encore Medical, LP or anything else in your household.
Get the Sunday Brief