DC Power Adapter for use with the LIFEPAK 12 defibrillator/monitor.
FDA device recall Z-0971-04 · posted 2004-07-20 · Terminated
Recall details
- Recalling firm
- Medtronic Physio Control Corp
- Reason for recall
- The DC Power Adapter may fail to charge LIFEPAK NiCd 2.4 AH batteries used with the LIFEPAK 12 defibrillator/monitor.
- Action taken
- On 5/5/04 the firm issued a letter to consignees advising of the problem and that a service representative will contact them regarding replacement of the DC Power Adapter.
- Root cause
- Other
- Status
- Terminated
- Product code
- LDD
- Quantity affected
- 1689
- Distribution
- The firm distributed devices to medical facilities, fire departments (first responders).
- Date initiated
- 2004-05-05
- Date posted
- 2004-07-20
- Date terminated
- 2005-01-06
- Location
- Redmond, WA
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| MEDTRONIC PHYSIO-CONTROL LIFEPAK 20 DEFIBRILLATOR/MONITOR/PACEMAKER (K012274) | Medtronic Physio-Control Corp. | 2002-02-05 |