Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway — Class II medical device recall Z-1519-2017
Terminated recall by Teleflex Medical, reported 2017-03-29, distributed nationwide. Labeling error
| Recall number | Z-1519-2017 |
|---|---|
| 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 | 2017-01-13 |
| Classified | 2017-03-21 |
| Reported by FDA | 2017-03-29 |
| Terminated | 2025-02-10 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, MX |
| Quantity | 7,600 eaches |
| Reason classes | labeling |
| Lot numbers | 16A14 |
| Model numbers | 123130, 123132 |
Product
Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, Catalog No. 123130 and 123132 Product Usage: To provide a patent airway for a patient with a blockage or potential blockage of the nasal cavity or nasopharynx.
Reason for recall
Labeling error
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-1519-2017. 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.