Device recall
Z-0307-03: Gambro ClinicalKit Safety Kit 15G, Catalog Number 0141080405C. Packaged 30 kits…
FDA device recall · Class II · Gambro Renal Products
Key facts
| Recall number (Z-number) | Z-0307-03 |
|---|---|
| Recall event | 25023 |
| Product | Gambro ClinicalKit Safety Kit 15G, Catalog Number 0141080405C. Packaged 30 kits per case. Each kit contains 2 Nipro Safetouch Safety Needles. |
| Recalling firm | Gambro Renal Products |
| Recall class | Class II |
| Status | Completed |
| FEI number | 1713683 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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