Device recall
Z-2064-2026: ERBEFLO 2, Endoscopy Pump Tubing/Cap Set, REF: 20325-222
FDA device recall · Class II · Erbe Medical, LLC
Key facts
| Recall number (Z-number) | Z-2064-2026 |
|---|---|
| Recall event | 98674 |
| Product | ERBEFLO 2, Endoscopy Pump Tubing/Cap Set, REF: 20325-222 |
| Product code | OCX |
| Recalling firm | Erbe Medical, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K190469 |
| FEI number | 3020712480 |
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