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Recall Observatory FDA recall evidence

Device product

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PULL Model/Catalog Number: 8180-24

Z-2352-2026

April 30, 2026

Class II

Product summary

Firm
Avanos Medical, Inc.
Event
Event 98907
Status
Ongoing
Classification
Class II
Quantity
1,205 kits
Official record key
device-enforcement:Z-2352-2026

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 10350770007868, Lot Numbers 30371319, 30374055, 30383058, 30386936

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.