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Snare, Surgical

FDA product code GAE · Class 1 · General, Plastic Surgery

74
Registered devices
150
Adverse events
3
Recalls
4
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2013-05-03Surgical Instrument Service And Savings, Inc.The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
2008-05-09Bard Peripheral Vascular IncThis action is being taken because the product has a potential for the handle to detach. The handle detachment may result in the device unable to retrieve the f
2008-05-09Bard Peripheral Vascular IncThis action is being taken because the product has a potential for the handle to detach. The handle detachment may result in the device unable to retrieve the f

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.