CORFLO NG/NI Pediatric Neonatal Feeding Tube w/ Anti-IV Connector — Class II medical device recall Z-0540-2021
Terminated recall by Avanos Medical, Inc., reported 2020-12-16, distributed in CA, CO, IL, LA, OH, VA. Detachment of the Male AIV Adaptor from the Y-Connector.
| Recall number | Z-0540-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Avanos Medical, Inc., Alpharetta, GA, United States |
| Recall initiated | 2020-10-16 |
| Classified | 2020-12-07 |
| Reported by FDA | 2020-12-16 |
| Terminated | 2022-09-30 |
| Distributed | CA, CO, IL, LA, OH, VA |
| Quantity | 710 units |
| Reason classes | device malfunction |
| Lot numbers | 0002983985 |
Product
CORFLO NG/NI Pediatric Neonatal Feeding Tube w/ Anti-IV Connector
Reason for recall
Detachment of the Male AIV Adaptor from the Y-Connector.
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-0540-2021. 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.