Device recall
Z-0719-2011: Bard CritiCore Monitor, Software Version 2.1, Catalog number 000002N, C.R. Bard…
FDA device recall · Class III · C.R. Bard, Inc., Urological Division
Key facts
| Recall number (Z-number) | Z-0719-2011 |
|---|---|
| Recall event | 57291 |
| Product | Bard CritiCore Monitor, Software Version 2.1, Catalog number 000002N, C.R. Bard, Inc., Covington, GA 30014. Intended for multiple uses as it is an electronic battery-operated monitor used in conjunction with a single-use disposable urine collection container and/or a temperature sensing Foley… |
| Product code | EXS |
| Recalling firm | C.R. Bard, Inc., Urological Division |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Feb 2, 2012 |
| FEI number | 1018233 |
At a glance
- None 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