Device recall
Z-0830-2021: Medisafe Distal Duck Kit and Duck Bag, Cleaner, ultrasonic, medical instrument…
FDA device recall · Class II · Steris Corporation
Key facts
| Recall number (Z-number) | Z-0830-2021 |
|---|---|
| Recall event | 86906 |
| Product | Medisafe Distal Duck Kit and Duck Bag, Cleaner, ultrasonic, medical instrument - Product Usage: intended to keep instruments moist during transportation between point of use and cleaning as an initial step of reprocessing. |
| Product code | FLG |
| Recalling firm | Steris Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 25, 2023 |
| FEI number | 1527821 |
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