medical MODERATE Updated 2026-10-14

GRI Medical & Electronic Technology Co., Ltd. recalls HALYARD Laparoscopy Comprehensive Pack II REF: 49332

See all recalls from GRI Medical & Electronic Technology Co., Ltd. →

Recalled Product

HALYARD Laparoscopy Comprehensive Pack II REF: 49332

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Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: 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

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for HALYARD Laparoscopy Comprehensive Pack →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

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