Device recall
Z-0178-06: Bard RespiShield * Closed Suction System with InnoValve * Endotracheal Start Kit…
FDA device recall · Class II · C.R. Bard, Inc., Urological Division
Key facts
| Recall number (Z-number) | Z-0178-06 |
|---|---|
| Recall event | 33780 |
| Product | Bard RespiShield * Closed Suction System with InnoValve * Endotracheal Start Kit * QTY 1 Unit * 14F/4.7mm * Sterile * Rx Only * C.R.Bard, Inc., Covington, GA 30014, 800-526-4455, www. bardmedical.com * Manufactured in Mexico. |
| Product code | BSY |
| Recalling firm | C.R. Bard, Inc., Urological Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 25, 2006 |
| FEI number | 1018233 |
At a glance
- None 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