Reported Oct 14, 2026 · Ongoing · Updated Oct 20, 2026
HALYARD Laparoscopy Comprehensive Pack II REF: 49332
GRI Medical & Electronic Technology Co., Ltd.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: GRI Medical & Electronic Technology Co., Ltd. · 1805 Honggao Road · Jia Xing, N/A · N/A
Is this the product you have?
- HALYARD
- Laparoscopy Comprehensive Pack II REF49332
- Lot codes and dates
- UDI-DI
10680651493320 (unit level)30680651493324 (case
- level) Lot NumbersGL25271CXA-Expiry
- Date2029/3/30
- GL25296CXA-Expiry Date2029/3/30
- GL26076CXA-Expiry Date2029/5/31
- UDI-DI
- Amount recalled
- 396 kits
Where it was sold
- Nationwide
- MS
Why it was recalled
Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter
This product could cause temporary or reversible health problems — stop using it.
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