The Recall Desk
HighFDA (Devices)·Z-2341-2026·Announced 2026-06-17

MIC Safety 7170-14 push PEG kits contain recalled lidocaine injection

MIC Safety PEG Kits, 14 Fr PUSH OTW, catalog number 7170-14, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 22 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, 14 Fr PUSH OTW, model/catalog number 7170-14, a feeding tube kit, is being recalled. The action covers 22 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 10350770007752, lot number 30370713. 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 number above, quarantine it, and follow the instructions issued by the manufacturer.

The recalled product

Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW Model/Catalog Number: 7170-14 Product Description: Feeding Tube Kit
Manufacturer
Avanos Medical, Inc.
Category
Medical Device — Gastrostomy kit
Hazard
Affected units
22

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 (2)

  • UDI-DI 10350770007752
  • Lot Number 30370713

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 →

Related recalls

Same manufacturer · Avanos Medical, Inc.

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Same hazard · contained drug recall

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