FDAFDA recall Z-0077-2027 · Oct 14, 2026
GRI Medical & Electronic Technology Co., Ltd.: HALYARD Laparoscopy Comprehensive Pack II REF: 49332 recall
Recall found
Product
HALYARD Laparoscopy Comprehensive Pack II REF: 49332
Reason for recall
Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- 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
- Quantity
- 396 kits
- Distribution
- US Nationwide distribution in the state of MS.
- Recalling firm
- GRI Medical & Electronic Technology Co., Ltd., Jia Xing, N/A
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-08-26
Source: openFDA enforcement record Z-0077-2027 · search recall number Z-0077-2027 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.