Device recall
Z-0932-2018: 241-McKesson Premium Skin Staple Remover Kit, Item #100123, McKesson I.V. Start…
FDA device recall · Class II · Cypress Medical Products LLC
Key facts
| Recall number (Z-number) | Z-0932-2018 |
|---|---|
| Recall event | 79341 |
| Product | 241-McKesson Premium Skin Staple Remover Kit, Item #100123, McKesson I.V. Start Kit, 100124-McKesson Suture Removal Kit, and 82-15 Cypress Medical Products Skin Staple Remover Kit. McKesson Item # 241, 100123, and 100124, Cypress Item # 82-15 Manual surgical instrument for general use. |
| Recalling firm | Cypress Medical Products LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 8, 2020 |
| FEI number | 1451040 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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