LeMaitre Vascular, Inc. — TufTex Over-the-Wire Embolectomy Catheter; Catalog Number: E1651-88;
Official product recall notices and clearly labeled enforcement reference records.
Reference record — not a live warning · enforcement-reference · official-source
Devices failed in process testing related to the amount of pull force it can sustain prior to the balloon components failing.
- Posted by source
- Source last updated
- Current version retrieved
- Provider
- FDA — device enforcement reference
- Location
- Burlington, MA, US
- hazard
- Devices failed in process testing related to the amount of pull force it can sustain prior to the balloon components failing.
- notice
- Periodic enforcement reference; not a real-time safety alert or a reliable recall-lifecycle tracker.
- product
- TufTex Over-the-Wire Embolectomy Catheter; Catalog Number: E1651-88;
- distribution
- US Nationwide distribution in the states of CA, FL, GA, KY, LA, NJ, OH, PA, SC.
- event number
- 99836
- manufacturer
- LeMaitre Vascular, Inc.
- recall number
- Z-0117-2027
- 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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