Device recall
Z-0227-04: Autovac TL. Autotransfusion System for Orthopedic Wound Drainage. The product is…
FDA device recall · Class III · Boehringer Laboratories Inc
Key facts
| Recall number (Z-number) | Z-0227-04 |
|---|---|
| Recall event | 27721 |
| Product | Autovac TL. Autotransfusion System for Orthopedic Wound Drainage. The product is shipped in cartons containing 6 units |
| Product code | CAC |
| Recalling firm | Boehringer Laboratories Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jan 20, 2004 |
| 510(k) numbers | K932093 |
| FEI number | 2518417 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database