Feeding Tube Kit Recall: Avanos CORFLO PEG ENFit
Announced 2026-06-17 · FDA
The FDA recall involves 22 CORFLO Safety PEG Kits with ENFit Connector (model 50-4320) distributed nationwide in the US. The recall is linked to lidocaine hydrochloride injection included into sterile kits due to a supplier issue. The recall numbers are UDI-DI 10350770007752 and Lot 30370713; no corrective action is listed.
| Brand | Avanos Medical, Inc. |
|---|---|
| Product | Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW Model/Catalog Number: 7170-14 Product Description: Feeding Tube Kit |
| Reason | Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. |
| Severity | moderate |
| Units affected | 49 |
| Distribution | US Nationwide distribution. |
| Agency | FDA |
| Recall / campaign no. | UDI-DI 10350770007752, Lot Number 30370713 |
WHAT YOU SHOULD DO
- Stop using the affected PEG kits immediately; check if you have a CORFLO Safety PEG Kit with ENFit Connector from Avanos, model 50-4320.
- Contact your healthcare provider or Avanos Medical for guidance and to arrange replacement or disposal; reference UDI-DI 10350770007752 and Lot 30370713.
- Do not modify or reuse the kit; follow the provider's disposal guidance.
- If you have used the kit and have concerns, contact your clinician or healthcare provider for advice.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.