TemporaryFDAOngoing
Can cause harm that is usually temporary.
HALYARD Laparoscopy Comprehensive Pack II REF: 49332
Check the device or its packaging for
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
- Why
- Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter
- Distributed
- US Nationwide distribution in the state of MS.
- Company
- GRI Medical & Electronic Technology Co., Ltd.
- Announced
- This is the date the recall was announced. A company may have started it weeks earlier.
- Recall began
Source: FDA record Z-0077-2027 · retrieved 2 October 2026
Read the official notice