Fresh Recalls

GRI Medical & Electronic Technology Co recalls

Recall found. GRI Medical & Electronic Technology Co is named in FDA Class II recall Z-0077-2027 covering HALYARD Laparoscopy Comprehensive Pack II REF. Hazard: Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter Identifying details: UDI-DI: 10680651493320 (unit level), 30680651493324 (case level) Lot Numbers: GL25271CXA-Expiry Date: 2029/3/30; GL25296CXA-Expiry Date: 2029/3/30; GL26076CXA-Expiry Date: 2029/5/31. Status: Ongoing.

Models with recalls

HALYARD Laparoscopy Comprehensive Pack II REF (1)

All GRI Medical & Electronic Technology Co recalls

FDA Class II · Medical device · October 14, 2026

HALYARD Laparoscopy Comprehensive Pack II REF recall — GRI Medical & Electronic Technology Co., Ltd.

Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter

Official ID Z-0077-2027 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 12:00 PM UTC.