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Pacemaker Battery

FDA product code DSZ · Class 3 · Cardiovascular

0
Registered devices
14
Adverse events
2
Recalls
0
510(k) clearances

Recent recalls

DateFirmReason
2012-12-05SynCardia Systems Inc.Syncardia Systems is recalling the Companion External Batteries used with the Companion 2 Driver System because they may potentially be at risk of thermal event
2010-05-24Maquet Cardiovascular, LLCVarious Hemashield products may develop glycerol droplets on the inner blister of the package if not stored under proper conditions, which could lead to the pro

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