Device recall
Z-2539-2024: Hookup Model/Catalog Number: DSD-110-HU0163 Product Description: Hookups provide…
FDA device recall · Class II · Steris Corporation
Key facts
| Recall number (Z-number) | Z-2539-2024 |
|---|---|
| Recall event | 94987 |
| Product | Hookup Model/Catalog Number: DSD-110-HU0163 Product Description: Hookups provide the interface between DSD Automated Endoscope Reprocessors ( AER ) and endoscopes, which allow perfusion of liquids dispensed by the AER to contact and high-level disinfect the channels of flexible endoscopes… |
| Product code | FEB |
| Recalling firm | Steris Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K092387 |
| FEI number | 1527821 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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