Recall Z-0227-04 ยท CAC Apparatus, Autotransfusion
Boehringer Laboratories Inc
Autovac TL. Autotransfusion System for Orthopedic Wound Drainage. The product is shipped in cartons containing 6 units
| Date | Dec 17, 2003 (initiated Nov 7, 2003) |
| Status | Terminated |
| Reason | Inadequate bond where the tube attaches to the inlet of the bulb. |
| Root cause | Other |
| Action | On 11/7/03, the recalling firm contact each account via visit by field representative. The representative informed the account of the problem and removed the product. |
| Quantity | 273 units |
| Distribution | The product was shipped to hospitals/medical centers in CT, IL, MD, MI, MS, NY, OK, PA, TN, and WA. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K932093 | AUTOVAC CLOSED WOUND AUTOTRANSFUSION SYSTEM,7920 S Boehringer Laboratories, Jul 6, 1994 |