Device recall
Z-1560-2015: PowerLoc MAX Safety Winged Infusion Set, Product Code 0132215 The PowerLoc MAX…
FDA device recall · Class II · Bard Access Systems
Key facts
| Recall number (Z-number) | Z-1560-2015 |
|---|---|
| Recall event | 70834 |
| Product | PowerLoc MAX Safety Winged Infusion Set, Product Code 0132215 The PowerLoc MAX Safety Winged Infusion Set is intended for use in the administration of fluids and drugs, as well as blood sampling through surgically implanted vascular ports. The PowerLoc MAX SWIS is also indicated for power injection… |
| Product code | FPA |
| Recalling firm | Bard Access Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 24, 2015 |
| 510(k) numbers | K073050 |
| FEI number | 3006260740 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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