FDA Medical Device Recalls (openFDA)
Guidant Corp-Cpi Division: Meridian Multiprogrammable Pacemaker, DDDR Model 1275
- Recall number
- Z-0888-03
- Recalling firm
- Guidant Corp-Cpi Division
- Product
- Meridian Multiprogrammable Pacemaker, DDDR Model 1275
- Status
- Terminated
- Initiated
- 2003-05-06
- Posted
- 2003-05-29
- Terminated
- 2005-11-18
- Reason
- In a rare circumstance (fallback mode when high-rate atrial activity is detected), the battery gauge can over-estimate battery life.
- Root cause
- Other
- Action
- An 'Important Pacemaker Follow-up Information' letter dated May 6, 2003 gave recommendations for avoiding the problem and indicated that updated software to prevent the problem would be introduced.
- Quantity
- not on file
- Distribution
- Nationwide in the United States and worldwide.
- Lot, serial or model codes
- All Serial numbers
- 510(k) numbers
- not on file
- PMA numbers
- ["P940031S011"]
- Product code
- DXY
- Firm FEI
- 2124215
- Firm city
- St Paul
- Firm state
- MN
- 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