Device recall
Z-1901-2020: Delfi Medical Innovations, VariFit Contour Cuffs, single use adult thigh cuff…
FDA device recall · Class II · Delfi Medical Innovations, Inc.
Key facts
| Recall number (Z-number) | Z-1901-2020 |
|---|---|
| Recall event | 84741 |
| Product | Delfi Medical Innovations, VariFit Contour Cuffs, single use adult thigh cuff, single port, single bladder, REF 9-9300-003. 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