HUDSON RCI — Class I medical device recall Z-2370-2015
Terminated recall by Teleflex Medical, reported 2015-08-26, distributed nationwide. The double swivel connector may crack or separate on the endobronchial tube.
| Recall number | Z-2370-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Research Triangle Park, NC, United States |
| Recall initiated | 2015-06-01 |
| Classified | 2015-08-19 |
| Reported by FDA | 2015-08-26 |
| Terminated | 2018-04-16 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, BE, BS, CA, CN, IN, JP, KR, MX, NZ, VN |
| Quantity | 188,195 units |
| Reason classes | packaging |
| Lot numbers | 01A1400436, 01C1400086, 01K1300254, 01L1300393, 01M1300212, 73A1500345, 73B1500272, 73C1500255, 73D1400096, 73D1400496, 73E1400269, 73F1400153, 73F1400352, 73G1400052, 73G1400288, 73H1400331, 73J1400401, 73L1400106, 73M1400208 |
Product
HUDSON RCI, Sheridan, SHER-I-SWIV and SHER-I-SWIV/FO Double Swivel, Rx Only, Sterile. Used temporarily to make rigid a flexible tracheal tube to aid its insertion into a patient.
Reason for recall
The double swivel connector may crack or separate on the endobronchial tube.
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-2370-2015. 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.