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Medical Device

HALYARD Laparoscopy Comprehensive Pack II REF: 49332

Recall date: 2026-10-14 · Source: FDA_DEVICE
Brand / Firm
GRI Medical & Electronic Technology Co., Ltd.
Product
HALYARD Laparoscopy Comprehensive Pack II REF: 49332
Reason for recall
Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter
Units affected
396 kits
Description
HALYARD Laparoscopy Comprehensive Pack II REF: 49332
View official recall notice →