Device recall
Z-2675-2011: Jet-Ventilator Catheter for Adults, 14G, STERILE, NO LATEX, REF 30-02-914-1, VBM…
FDA device recall · Class II · VBM Medical Inc.
Key facts
| Recall number (Z-number) | Z-2675-2011 |
|---|---|
| Recall event | 58807 |
| Product | Jet-Ventilator Catheter for Adults, 14G, STERILE, NO LATEX, REF 30-02-914-1, VBM Medizintechnik GmbH, Einsteinstrasse 1 7212 Sulz a.N. Germany Allows a safe and atraumatic transtracheal access for oxygenation/ventilation with a manual jet ventilator or an automatic high frequency jet ventilator. |
| Product code | BTO |
| Recalling firm | VBM Medical Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 14, 2012 |
| 510(k) numbers | K955461 |
| FEI number | 3003316541 |
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