Sheridan/CF Cuffed Tracheal Tube — Class II medical device recall Z-0799-2015
Terminated recall by Teleflex Medical, reported 2014-12-24. Product Labeling; Units from the affected lot indicates that it contains a size 8mm tracheal tube but may cont
| Recall number | Z-0799-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Durham, NC, United States |
| Recall initiated | 2014-11-12 |
| Classified | 2014-12-12 |
| Reported by FDA | 2014-12-24 |
| Terminated | 2017-10-13 |
| Countries outside the US | BE, CA, JP |
| Quantity | 14,000 units |
| Reason classes | labeling |
| Lot numbers | 01A1400211 |
Product
Sheridan/CF Cuffed Tracheal Tube, Sterile, Rx only, Teleflex Medical, Research Triangle Park, NC 27708. Designed for oral and nasal intubation and are indicated for airway management.
Reason for recall
Product Labeling; Units from the affected lot indicates that it contains a size 8mm tracheal tube but may contain a size 7.5mm tracheal 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-0799-2015. 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.