GRI Medical & Electronic Technology Co., Ltd. recalls HALYARD Laparoscopy Comprehensive Pack II REF: 49332
- Recalling company
- GRI Medical & Electronic Technology Co., Ltd.
- Product
- HALYARD Laparoscopy Comprehensive Pack II REF: 49332
- Reason
- Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Aug 26, 2026
- Reported
- Oct 14, 2026
- Distribution
- US Nationwide distribution in the state of MS.
- Status
- Ongoing
- Quantity
- 396 kits
- Lot / codes
- 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
- Company location
- Jia Xing, N/A
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0077-2027
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0077-2027 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.