Hudson RCI — Class II medical device recall Z-2251-2017
Terminated recall by Teleflex Medical, reported 2017-06-14, distributed in CA, CT, FL, IL, IN, MD, MI, MN…. Incorrect labeling; the box label indicates Pediatric, the product insert indicates an Adult device.
| Recall number | Z-2251-2017 |
|---|---|
| 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 | 2017-05-09 |
| Classified | 2017-06-07 |
| Reported by FDA | 2017-06-14 |
| Terminated | 2025-01-16 |
| Distributed | CA, CT, FL, IL, IN, MD, MI, MN, MO, MS, NC, NJ, NV, NY, OH, PA, TX, VA, WI, WV |
| Quantity | 1,150 units |
| Reason classes | labeling |
| Lot numbers | 74J1603122, 74K1601506, 74K1602306, 74L16006 |
Product
Hudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx only,
Reason for recall
Incorrect labeling; the box label indicates Pediatric, the product insert indicates an Adult device.
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-2251-2017. 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.