FDA Device recall Z-0540-2021
CORFLO NG/NI Pediatric Neonatal Feeding Tube w/ Anti-IV Connector
- FDA Device
- Class II
- terminated
- Published 2020-12-16
On 2020-12-16 the FDA classified a Class II recall of CORFLO NG/NI Pediatric Neonatal Feeding Tube w/ Anti-IV Connector by Avanos Medical, citing detachment of the Male AIV Adaptor from the Y-Connector.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0540-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-10-16 |
| Published | 2020-12-16 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Avanos Medical |
| Distribution | CA, CO, IL, LA, OH, VA |
Product
CORFLO NG/NI Pediatric Neonatal Feeding Tube w/ Anti-IV Connector
Reason
Detachment of the Male AIV Adaptor from the Y-Connector.
Identifiers
| code_info | Product Code:20-1225AIV, Lot Number: 0002983985 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0540-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.