Maquet Datascope Corp: 6 recalls on record
Recalls filed with 1 agency: FDA (6).
First recall on record: May 28, 2014. Most recent: November 7, 2018.
Risk classification: Class I: 6
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| November 7, 2018 | FDA | Cardiosave Rescue IABP, Part Number 0998-UC-0800-83Z-0100-2019 | Z-0100-2019 |
| September 13, 2017 | FDA | CS 100 Intra-Aortic Balloon Pump. It supports the heart's left ventricle by increasing…Z-3086-2017 | Z-3086-2017 |
| August 2, 2017 | FDA | CS 100 Intra-Aortic Balloon PumpZ-2737-2017 | Z-2737-2017 |
| August 2, 2017 | FDA | CS 300 Intra-Aortic Balloon PumpZ-2738-2017 | Z-2738-2017 |
| August 2, 2017 | FDA | CS 100i Intra-Aortic Balloon PumpZ-2736-2017 | Z-2736-2017 |
| May 28, 2014 | FDA | Datascope System 98/98xt, CS 100/CS100i and CS 300 Intra-Aortic Balloon Pump. The Int…Z-1523-2014 | Z-1523-2014 |
Questions about this company
- How many recalls does Maquet Datascope Corp have?
- Recalert has 6 U.S. recalls on record for Maquet Datascope Corp, published between May 28, 2014 and November 7, 2018.
- What was the most recent Maquet Datascope Corp recall?
- FDA recall Z-0100-2019, published November 7, 2018: Cardiosave Rescue IABP, Part Number 0998-UC-0800-83
- Which agencies have handled Maquet Datascope Corp recalls?
- Maquet Datascope Corp appears as the recalling firm in recalls from: FDA (6).
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