The Recall Desk
HighFDA (Devices)·Z-2345-2026·Announced 2026-06-17

MIC Safety 20 Fr pull PEG kits contain recalled lidocaine injection

MIC Safety PEG Kits, 20 Fr PULL, catalog number 7180-20, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 3,184 kits 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 MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit, 20 Fr PULL, model/catalog number 7180-20, is being recalled. The action covers 3,184 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 10350770007783, spanning the lot numbers listed in the recall notice including 30371313, 30371314, 30373295 and 30373296. 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
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL Model/Catalog Number: 7180-20
Manufacturer
Avanos Medical, Inc.
Category
Medical Device — Gastrostomy kit
Hazard
Affected units
3,184

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 (8)

  • UDI-DI 10350770007783
  • Lot Numbers 30371313
  • 30371314
  • 30373295
  • 30373296
  • 30374832
  • 30378735
  • 80403340

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 →

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Same manufacturer · Avanos Medical, Inc.

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