RUSCH Endotracheal Tube oral/nasal Murphy Eye — Class II medical device recall Z-2322-2021
Terminated recall by Teleflex Medical Europe Ltd, reported 2021-08-25, distributed nationwide. The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained f
| Recall number | Z-2322-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical Europe Ltd, Athlone, N/A, Ireland |
| Recall initiated | 2021-07-16 |
| Classified | 2021-08-19 |
| Reported by FDA | 2021-08-25 |
| Terminated | 2026-07-24 |
| Distributed | Nationwide (US) |
| Quantity | 638,220 units |
| Lot numbers | KME20J2802, KME20J2998, KME20J2999, KME20J3284, KME20J3341, KME20K0036, KME20K0052, KME20K0061, KME20K0180, KME20K0181, KME20K0211, KME20K0212, KME20K0259, KME20K0435, KME20K0436, KME20K0437, KME20K0462, KME20K0463, KME20K0464, KME20K0504, KME20K0585, KME20K0600, KME20K0677, KME20K0683, KME20K0881, KME20K0923, KME20K0977, KME20K0978, KME20K1007, KME20K1112, KME20K1113, KME20K1114, KME20K1273, KME20K1434, KME20K1513, KME20K1583, KME20K1809, KME20K1831, KME20K2166, KME20K2168 and 308 more |
Product
RUSCH Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF numbers: a) 112082050 b) 112082055 c) 112082060 d) 112082065 e) 112082070 f) 112082075 g) 112082080 h) 112082085 i) 112082090 j) 112082095 k) 112082100
Reason for recall
The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.
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-2322-2021. 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.