Device recall
Z-0493-2015: GuardIVa Antimicrobial Hemostatic IV Dressing, REF FP-23-AD008, Manufacturer…
FDA device recall · Class II · Bard Access Systems
Key facts
| Recall number (Z-number) | Z-0493-2015 |
|---|---|
| Recall event | 69683 |
| Product | GuardIVa Antimicrobial Hemostatic IV Dressing, REF FP-23-AD008, Manufacturer: Bard Access Systems, Inc. USA. Product Code FP23AD006. |
| Product code | FRO |
| Recalling firm | Bard Access Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 12, 2015 |
| FEI number | 3006260740 |
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