Home › Device types › DSZ
Pacemaker Battery
FDA product code DSZ · Class 3 · Cardiovascular
0
Registered devices
14
Adverse events
2
Recalls
0
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2012-12-05 | SynCardia 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 |
| 2010-05-24 | Maquet Cardiovascular, LLC | Various 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 |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
