Gri Medical & Electronic Technology Co., Ltd.: Laparoscopy Kit
- Recalling firm
- 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
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-08-26
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution in the state of MS.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/33637dd6-6222-42ef-8e2f-d17519cef95f