Device recall
Z-2327-2012: Bard Foley procedural trays packaged in breather bags. The product is packaged…
FDA device recall · Class II · C.R. Bard, Inc., Urological Division
Key facts
| Recall number (Z-number) | Z-2327-2012 |
|---|---|
| Recall event | 62774 |
| Product | Bard Foley procedural trays packaged in breather bags. The product is packaged ten units in each shipper box, and are sold sterile for single use. Used to catheterize patients. The finished trays are sold in Tyvek breather bags. |
| Product code | EZC |
| Recalling firm | C.R. Bard, Inc., Urological Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 7, 2013 |
| 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