ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes &… — Class II medical device recall Z-2062-2026
Ongoing recall by Erbe Medical, LLC, reported 2026-05-13, distributed nationwide. Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment conne
| Recall number | Z-2062-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Erbe Medical, LLC, Tempe, AZ, United States |
| Recall initiated | 2026-03-31 |
| Classified | 2026-05-01 |
| Reported by FDA | 2026-05-13 |
| Distributed | Nationwide (US) |
| Quantity | 260,962 |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 04065655000375, 04065655000405, 04065655000436, 04065655000689, 04065655001006, 04065655001099 |
| Lot numbers | W4464507, W4464512, W4464514, W4464515, W4464516, W4464517, W4465114, W4465115, W4465116, W4465702, W4465709, W4465991, W4466004, W4466021, W4466266, W4466267, W4466268, W4466269, W4466271, W4466272, W4466273, W4466275, W4466278, W4466279, W4466813, W4466814, W4466815, W4466816, W4467049, W4467051, W4467055, W4467056, W4467057, W4467058, W4467059, W4467678, W4467679, W4467680, W4467681, W4467682 and 108 more |
| Model numbers | 20325-206, 20325-207, 20325-208, 20325-239, 20325-240, 20325-248 |
Product
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 Olympus Scopes, REF: 20325-206; Hybrid CO2 Tubing/Cap Set for Pentax Scopes, REF: 20325-207; ERBEFLO CleverCap Hybrid CO2 Tubing/Cap Set for Fujifilm Scopes, REF: 20325-248; Hybrid CO2 Tubing/Cap Set for Fujinon Scopes, REF: 20325-208
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 under unsupported third-party connector use conditions, which may lead to water aspiration, which may progress to aspiration pneumonia, acute respiratory distress syndrome, or respiratory failure.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2062-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.