Device recall
Z-0157-06: Boehringer Suction Regulator Model number 3714
FDA device recall · Class II · Boehringer Laboratories, Inc.
Key facts
| Recall number (Z-number) | Z-0157-06 |
|---|---|
| Recall event | 32810 |
| Product | Boehringer Suction Regulator Model number 3714 |
| Product code | KDP |
| Recalling firm | Boehringer Laboratories, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 16, 2005 |
| 510(k) numbers | K853095 |
| FEI number | 2518417 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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