Official recall notice

FDA DeviceClass IINotable

HALYARD Laparoscopy Comprehensive Pack II Recall (Oct 2026)

Product: HALYARD Laparoscopy Comprehensive Pack II REF: 49332

Recall date
2026-10-14
FDA class
Class II

Why it was recalled

Hazard

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

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Product description

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

Affected products

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

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