Sterile Sheridan/HVT Cuffed — Class II medical device recall Z-1938-2016
Terminated recall by Teleflex Medical, reported 2016-06-15, distributed in AL, AZ, CO, FL, GA, IA, ID, IL…. The labeling of some units indicates that it contains a size 7mm tracheal tube, but may contain a size 7.5mm t
| Recall number | Z-1938-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Research Triangle Park, NC, United States |
| Recall initiated | 2016-05-05 |
| Classified | 2016-06-09 |
| Reported by FDA | 2016-06-15 |
| Terminated | 2017-08-25 |
| Distributed | AL, AZ, CO, FL, GA, IA, ID, IL, IN, KY, LA, MA, MD, MI, MN, MO, NC, NY, OK, PA, RI, TX, UT |
| Quantity | 6,390 units |
| Reason classes | labeling |
| Lot numbers | 73F1500606 |
| Model numbers | 7.0, V5-10314 |
Product
Sterile Sheridan/HVT Cuffed, Murphy Eye, Tracheal Tube, Ref: V5-10314, ID: 7.0 mm, Rx Only, Manufactured by: Teleflex Incorporated. A tracheal tube is inserted into a patients mouth or nose for airway management.
Reason for recall
The labeling of some units indicates that it contains a size 7mm 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-1938-2016. 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.