Thoratec Corporation: 5 recalls on record
Recalls filed with 1 agency: FDA (5).
First recall on record: April 2, 2014. Most recent: May 31, 2017.
Risk classification: Class I: 5
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| May 31, 2017 | FDA | HeartMate¿ II LVAS with Pocket Controller; 106762 - HMII POCKET CONTROLLER, NA; UDI: 0…Z-2053-2017 | Z-2053-2017 |
| April 2, 2014 | FDA | HeartMate II LVAD Pump and Pock Controller Kit; Product Usage: HeartMate II is a me…Z-229-2014 | Z-229-2014 |
| April 2, 2014 | FDA | HeartMate II System Controller Product Usage: HeartMate II is a mechanical device tha…Z-1228-2014 | Z-1228-2014 |
| April 2, 2014 | FDA | HeartMate II Implant Kit with Pocket Controller; with sealed grafts (NAm) with sealed g…Z-1227-2014 | Z-1227-2014 |
| April 2, 2014 | FDA | Heart Mate II Pocket Controllers removed from packaging Product Usage: HeartMate II…Z-1230-2014 | Z-1230-2014 |
Questions about this company
- How many recalls does Thoratec Corporation have?
- Recalert has 5 U.S. recalls on record for Thoratec Corporation, published between April 2, 2014 and May 31, 2017.
- What was the most recent Thoratec Corporation recall?
- FDA recall Z-2053-2017, published May 31, 2017: HeartMate¿ II LVAS with Pocket Controller; 106762 - HMII POCKET CONTROLLER, NA; UDI: 00813024011286 Intended to provide hemodynamic support in patients with end-stage, refractory left ventricul…
- Which agencies have handled Thoratec Corporation recalls?
- Thoratec Corporation appears as the recalling firm in recalls from: FDA (5).
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