FDA Medical Device Recalls (openFDA)
Medtronic Physio Control Corp: LIFEPAK 12 defibrillator/monitor.
- Recall number
- Z-0938-04
- Recalling firm
- Medtronic Physio Control Corp
- Product
- LIFEPAK 12 defibrillator/monitor.
- Status
- Terminated
- Initiated
- 2004-04-05
- Posted
- 2004-07-20
- Terminated
- 2005-01-06
- Reason
- Potential for display to go blank due to an electrical component that may fail due to mechanical shock of vibration of the defibrillator.
- Root cause
- Other
- Action
- Letters dated April 2004 were sent to customers on 4/6/04. The letter explains that a service representative will visit the customer and check the capacitor.
- Quantity
- 2885
- Distribution
- Devices were distributed to hospitals and medical centers throughout the US. The firm also distributed units internationally.
- Lot, serial or model codes
- Part numbers VLP12, UVLP12, EVLP12, DVLP12, AVLP12, and any of these may have five to eight digits after the base number. Serial numbers can be obtained from the firm or FDA''s Seattle District Recall Coordinator
- 510(k) numbers
- ["K012274"]
- PMA numbers
- not on file
- Product code
- LDD
- Firm FEI
- 3015876
- Firm city
- Redmond
- Firm state
- WA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28