HALYARD Laparoscopy Comprehensive Pack II REF: 49332 recall (GRI Medical & Electronic Technology Co., Ltd.)
Medical deviceClass IIOngoing
Summary: GRI Medical & Electronic Technology Co., Ltd. is recalling HALYARD Laparoscopy Comprehensive Pack II REF: 49332. Reason: Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter.
What is being recalled
HALYARD Laparoscopy Comprehensive Pack II REF: 49332
Why
Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
US Nationwide distribution in the state of MS. (states named: Mississippi)
How to tell if yours is affected
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 to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-0077-2027 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | August 26, 2026 |
| Reported | October 14, 2026 |
| Company | GRI Medical & Electronic Technology Co., Ltd. |
| Company location | Jia Xing, N/A, China |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 396 kits |
More recalls from GRI Medical & Electronic Technology Co., Ltd. · all medical device recalls · recalls from August 2026