GRI Medical & Electronic Technology Co., Ltd. — HALYARD Laparoscopy Comprehensive Pack II REF: 49332
Official product recall notices and clearly labeled enforcement reference records.
Reference record — not a live warning · enforcement-reference · official-source
Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter
- Posted by source
- Source last updated
- Current version retrieved
- Provider
- FDA — device enforcement reference
- Location
- US
- hazard
- Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter
- notice
- Periodic enforcement reference; not a real-time safety alert or a reliable recall-lifecycle tracker.
- product
- HALYARD Laparoscopy Comprehensive Pack II REF: 49332
- distribution
- US Nationwide distribution in the state of MS.
- event number
- 99813
- manufacturer
- GRI Medical & Electronic Technology Co., Ltd.
- recall number
- Z-0077-2027
- source status
- Open, Classified
- freshness minutes
- 180
Source use policy · openFDA reference data; not a real-time public alert service
Update history (1 recent revisions)
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