Device recall
Z-1902-2020: DELFI SINGLE USE VARIFIT TOURNIQUET CUFF SINGLE PORT SINGLE BLADDER CONTOUR…
FDA device recall · Class II · Delfi Medical Innovations, Inc.
Key facts
| Recall number (Z-number) | Z-1902-2020 |
|---|---|
| Recall event | 84741 |
| Product | DELFI SINGLE USE VARIFIT TOURNIQUET CUFF SINGLE PORT SINGLE BLADDER CONTOUR THIGH CUFF WITH MATHCING LIMP PROTECTION SLEEVE Rx Only, Sterile |
| Product code | KCY |
| Recalling firm | Delfi Medical Innovations, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 22, 2022 |
| FEI number | 3003748933 |
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