MVP-10 Pediatric/ Neonatal Volume Ventilator
FDA device recall Z-0300-04 · posted 2004-01-06 · Terminated
Recall details
- Recalling firm
- Bio-Med Devices, Inc.
- Reason for recall
- Two way relief valve may fail to activate at the low negative pressure of -3cm H2O.
- Action taken
- Bio Med Devices notified accounts by telephone on 11/7/03, to return the device for replacement and correction.
- Root cause
- Other
- Status
- Terminated
- Product code
- MNT
- Quantity affected
- 3 units
- Distribution
- ID, PA, TX
- Date initiated
- 2003-11-07
- Date posted
- 2004-01-06
- Date terminated
- 2016-02-01
- Location
- Guilford, CT
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