Skip to content
Recall Observatory FDA recall evidence

Device product

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL Model/Catalog Number: 7180-20

Z-2345-2026

April 30, 2026

Class II

Product summary

Firm
Avanos Medical, Inc.
Event
Event 98907
Status
Ongoing
Classification
Class II
Quantity
3,184 kits
Official record key
device-enforcement:Z-2345-2026

Official wording

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

Code information: UDI-DI 10350770007783, Lot Numbers 30371313, 30371314, 30373295, 30373296, 30374832, 30378735, 80403340

Distribution pattern: US Nationwide distribution.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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