International safety notice
Recall of Li-Ion Battery used with Maquet CARDIOSAVE Hybrid IABP / Rescue IABP, Maquet Getinge Group
Germany / BfArM · DEU · Feb 9, 2017
Key facts
| Title | Recall of Li-Ion Battery used with Maquet CARDIOSAVE Hybrid IABP / Rescue IABP, Maquet Getinge Group |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of Li-Ion Battery used with Maquet CARDIOSAVE Hybrid IABP / Rescue IABP, Maquet Getinge Group |
| Manufacturer | Recall of Li-Ion Battery used with Maquet CARDIOSAVE Hybrid IABP / Rescue IABP, Maquet Getinge Group |
| Models | 1-800-332-1088, 0146-00-0097, ML-0635, 1-800-FDA-0178 |
| Date | Feb 9, 2017 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1