CLASS II ONGOING Device recall · Reported 17 Jun 2026 · FDA Enforcement Report

MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit PUSH OTW recalled

Avanos Medical is recalling MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit PUSH OTW, distributed nationwide in the US. The recall was initiated on 30 Apr 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Code: Model No 7170-20, UDI-DI 10350770007776, Lot Numbers 30370714, 30373419, 30374048, 30378746

Quantity recalled901 kits

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-2342-2026
FDA event ID: 98907
Recalling firm: Avanos Medical, Alpharetta, GA
Classification: Class II
Status: Ongoing
Recall initiated: 30 Apr 2026
FDA classified: 5 Jun 2026
Reported: 17 Jun 2026
Type: Voluntary: Firm initiated
Customers notified by: N/A
Reason category: Sterility
Device type: Surgical Instruments

Timeline

30 Apr 2026	Recall initiated by company
5 Jun 2026	Classified by FDA	+36 days
17 Jun 2026	Published in enforcement report	+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW Model/Catalog Number: 7170-20 Product Description: Feeding Tube Kit Component: No

Where it was distributed

US Nationwide distribution.

Nationwide

Questions about this recall

Why was it recalled?

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Which lots are affected?

Lot Code: Model No 7170-20, UDI-DI 10350770007776, Lot Numbers 30370714, 30373419, 30374048, 30378746

Where was it sold?

US Nationwide distribution.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

19 other products · FDA event 98907

This product is part of a recall event; the main page for the event is Corflo* Safety PEG Kit with ENFit¿ Connector recalled by Avanos Medical.

Reported	Class	Recall	Company	Reason	Where
17 Jun 2026	CLASS II	Corflo* Safety PEG Kit with ENFit¿ Connector recalled by Avanos Medical	Avanos Medical	Sterility	Nationwide
17 Jun 2026	CLASS II	MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit PUSH OTW recalled	Avanos Medical	Sterility	Nationwide
17 Jun 2026	CLASS II	Corflo* Safety PEG Kit with ENFit¿ Connector recalled by Avanos Medical	Avanos Medical	Sterility	Nationwide
17 Jun 2026	CLASS II	MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit recalled	Avanos Medical	Sterility	Nationwide
17 Jun 2026	CLASS II	MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit PULL recalled	Avanos Medical	Sterility	Nationwide
17 Jun 2026	CLASS II	Corflo Safety PEG Kit recalled by Avanos Medical	Avanos Medical	Sterility	Nationwide
17 Jun 2026	CLASS II	MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit PULL recalled	Avanos Medical	Sterility	Nationwide
17 Jun 2026	CLASS II	Corflo* Safety PEG Kit recalled by Avanos Medical	Avanos Medical	Sterility	Nationwide
17 Jun 2026	CLASS II	Corflo* Safety PEG Kit with ENFit¿ Connector recalled by Avanos Medical	Avanos Medical	Sterility	Nationwide
17 Jun 2026	CLASS II	MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit recalled	Avanos Medical	Sterility	Nationwide
17 Jun 2026	CLASS II	MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit recalled	Avanos Medical	Sterility	Nationwide
17 Jun 2026	CLASS II	MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit recalled	Avanos Medical	Sterility	Nationwide
17 Jun 2026	CLASS II	Corflo* Safety PEG Kit recalled by Avanos Medical	Avanos Medical	Sterility	Nationwide
17 Jun 2026	CLASS II	Corflo* Safety PEG Kit recalled by Avanos Medical	Avanos Medical	Sterility	Nationwide
17 Jun 2026	CLASS II	Corflo Safety PEG Kit with ENFit Connector recalled by Avanos Medical	Avanos Medical	Sterility	Nationwide
17 Jun 2026	CLASS II	MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit recalled	Avanos Medical	Sterility	Nationwide
17 Jun 2026	CLASS II	MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit PULL recalled	Avanos Medical	Sterility	Nationwide
17 Jun 2026	CLASS II	MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit recalled	Avanos Medical	Sterility	Nationwide
17 Jun 2026	CLASS II	MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit PUSH OTW recalled	Avanos Medical	Sterility	Nationwide

More recalls from Avanos Medical

All 57

Reported	Class	Recall	Company	Reason	Where
17 Jun 2026Device	CLASS II	MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit PUSH OTW recalled	Avanos Medical	Sterility	Nationwide
17 Jun 2026Device	CLASS II	MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit recalled	Avanos Medical	Sterility	Nationwide
17 Jun 2026Device	CLASS II	MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit PULL recalled	Avanos Medical	Sterility	Nationwide
17 Jun 2026Device	CLASS II	MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit recalled	Avanos Medical	Sterility	Nationwide
17 Jun 2026Device	CLASS II	Corflo Safety PEG Kit with ENFit Connector recalled by Avanos Medical	Avanos Medical	Sterility	Nationwide

Other Surgical Instruments recalls

All 3,809

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9 Sep 2026Device	CLASS II	Medline Convenience Kits: IV Start KIT recalled by Medline Industries	Medline Industries	Sterility	Nationwide
9 Sep 2026Device	CLASS II	Medline Convenience Kits containing BD ChloraPrep Clear recalled	Medline Industries	Packaging Defects	Nationwide
2 Sep 2026Device	CLASS II	Medline convenience kits labeled as: Open Heart Pack, Medline Kit recalled	Medline Industries	Other	Nationwide
2 Sep 2026Device	CLASS II	Medline convenience kits labeled as: GYN Robotic CDS, Medline Kit recalled	Medline Industries	Other	Nationwide
2 Sep 2026Device	CLASS II	Linvatec Genesys CrossFT Suture Anchor with Disposable Driver recalled	ConMed	Other	Nationwide