The Recall Desk
HighFDA (Devices)·Z-2334-2026·Announced 2026-06-17

CORFLO Safety PEG kit 30-5320 contains recalled lidocaine injection

CORFLO Safety PEG Kits, catalog number 30-5320, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 61 kits are affected.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: FDA Class II recall where an injectable drug with unresolved quality issues was packed into sterile kits, a risk of harm with no injuries reported.

Plain-English summary

The CORFLO Safety PEG Kit, model/catalog number 30-5320, is being recalled. The action covers 61 kits.

The stated reason is that lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, was included in sterile kits and sets. The FDA classified the action as Class II.

Affected product is UDI-DI 10350770007554, spanning the lot numbers listed in the recall notice including 30365227, 30368642, 30374529, 30376099 and 30380696. Distribution was nationwide in the United States. The kits are supplied to healthcare facilities rather than sold to consumers.

Facilities should identify affected stock using the catalog number, UDI-DI and lot numbers in the recall notice, quarantine it, and follow the instructions issued by the manufacturer.

The recalled product

Product
Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 30-5320
Affected units
61

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (7)

  • UDI-DI 10350770007554
  • Lot Numbers 30365227
  • 30368642
  • 30374529
  • 30376099
  • 30380696
  • and 30387248

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 20 recalled by Avanos Medical, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 20 products in this recall →