Drug recall
ERBEFLO 2, Endoscopy Pump Tubing/Cap Set, REF: 20325-222
FDA recall event 98674 · Class II · Erbe Medical, LLC
Key facts
| Event ID | 98674 |
|---|---|
| Recall numbers | Z-2062-2026, Z-2063-2026, Z-2064-2026 |
| Recalling firm | Erbe Medical, LLC |
| Product type | Devices |
| Products | ERBEFLO 2, Endoscopy Pump Tubing/Cap Set, REF: 20325-222, ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2 Tubing/Cap Set for Olympus Scopes & UCR, REF: 20325-240; Hybrid CO2 Tubing/Cap Set for…, ERBEFLO CleverCap: Hybrid Tubing/Cap Set for Olympus Scopes, 20325-201; ERBEFLO CleverCap Hybrid Tubing/Cap Set for Fujifilm Scopes, REF: 20325-203; |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible to unintended water flow from distal tip… |
| Initiation date | Mar 31, 2026 |
| Report date | May 13, 2026 |
| City | Tempe |
| State | AZ |
| Country | United States |
| FEI number | 3020712480 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: