Jia Xing, N/A, China
GRI Medical & Electronic Technology Co., Ltd. recalls
1 recall recorded since 2018, most recently on 26 August 2026. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 26 August 2026
- Reason
- Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter
- Distribution
- US Nationwide distribution in the state of MS.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0077-2027
- HALYARD Laparoscopy Comprehensive Pack II REF: 49332
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.