Device recall
Z-2463-2023: SurgiCount+ Software Application-indicated as an adjunctive technology for…
FDA device recall · Class II · Stryker Corporation
Key facts
| Recall number (Z-number) | Z-2463-2023 |
|---|---|
| Recall event | 92713 |
| Product | SurgiCount+ Software Application-indicated as an adjunctive technology for augmenting the manual process of counting, displaying and recording the number of RFID-tagged absorbent articles used during surgical procedures Product Code: 0694-002-090; |
| Product code | PVZ |
| Recalling firm | Stryker Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3015967359 |
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