Recall Z-1376-2008 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Biomet, Inc.
Biomet Vanguard DCM CR Tibial Bearing, 14MM x 79/83MM, CR STD bearing, sterile, Biomet Orthopedics, Inc., Warsaw, IN; Part 183464.
| Date | Jul 25, 2008 (initiated Feb 12, 2008) |
| Status | Terminated |
| Reason | Mislabeled: The packaging of the two products was mixed up, resulting in the products being labeled with an incorrect size. If implanted, the product may not fit properly, which could require repeat surgery. The problem could also result in a delay in the procedure. |
| Root cause | Packaging process control |
| Action | Distributors were notified via recall letter (Urgent Medical Device Removal Notice) dated 2/12/08 to locate the devices in their possession and at hospital sites, discontinue use, and return them to Biomet. Hospitals having received the devices will be provided with a recall letter dated 2/12/08 which describes the nature of the problem and the removal of these instruments. A third letter dated 2/12/08 was provided for implanting physicians. |
| Quantity | 8 |
| Distribution | Worldwide: USA and Australia |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K023546 | MAXIM ACCEL KNEE SYSTEM Biomet, Inc., Jan 17, 2003 |