Device recall
Z-1323-2026: Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE…
FDA device recall · Class I · Medline Industries, LP
Key facts
| Recall number (Z-number) | Z-1323-2026 |
|---|---|
| Recall event | 98277 |
| Product | Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE Catheter 9F x 90cm D087031RH 20197344019554 |
| Product code | OWQ |
| Recalling firm | Medline Industries, LP |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K232130 |
| FEI number | 1417592 |
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