Class I — TELEFLEX LLC
| Recalling firm | Teleflex |
|---|---|
| Registered facility | View this company's 9 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class I |
| Status | Ongoing |
| Reason | Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. |
| Product | Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 1700100 |
| Quantity | 190 units |
| Distribution | US Nationwide distribution including Puerto Rico. |
| Initiated | 2023-05-25 |
| Classified | 2023-06-29 |
| Recall number | Z-1860-2023 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class I recall — TELEFLEX LLC (Z-1860-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/92373/
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