FDA Device recall Z-1936-2023
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382045
- FDA Device
- Class I
- ongoing
- Published 2023-07-05
On 2023-07-05 the FDA classified a Class I recall of Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382045 by Teleflex, citing reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1936-2023 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2023-05-25 |
| Published | 2023-07-05 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Teleflex |
| Distribution | US |
Product
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382045
Reason
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Identifiers
| code_info | UDI/DI 14026704340825, Batch Numbers: 18GG15, 18GG26, 18HG25, 18IG04, 18IG14, 18IG29, 18JG08, 18JG35, 18KG08, 18LG01,…UDI/DI 14026704340825, Batch Numbers: 18GG15, 18GG26, 18HG25, 18IG04, 18IG14, 18IG29, 18JG08, 18JG35, 18KG08, 18LG01, 19BG12, 19DT13, 19GT35, 19KT13, 19LT50, 20CT11, 20FT43, 20GT22, 20GT37, KME20H0783, KME20J2818, KME20J2819, KME20J2846, KME20K0469, KME20M1075, KME21B0085, KME21B1134, KME21B1828, KME21C1577, KME21C2244, KME21C2444, KME21D2950, KME21D2951, KME22D2158, KME22D2478, KME22E0295, KME22E0608, KME22E0909, KME22E0911, KME22E1313, KME22E2291, KME22J3174, KME22K2663, KME22K2686, KME22M0003, KME22M1623, KME23A2310, KME23B0782 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1936-2023%22
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