Device recall
Z-0271-2012: TUM-E-VAC REF 2075, Rx ONLY, NON STERILE --- Ethox International, Buffalo, NY…
FDA device recall · Class III · Ethox International, Inc.
Key facts
| Recall number (Z-number) | Z-0271-2012 |
|---|---|
| Recall event | 60374 |
| Product | TUM-E-VAC REF 2075, Rx ONLY, NON STERILE --- Ethox International, Buffalo, NY 14204, USA --- Intended use: gastric lavage |
| Product code | KNT |
| Recalling firm | Ethox International, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 28, 2011 |
| 510(k) numbers | K812648 |
| FEI number | 1314417 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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