FDA Medical Device Recalls (openFDA)
Philips Medical Systems: HeartStart Pads Pediatric Plus, Pediatric Plus Multifunction Defibrillation Electrode Pads Model M3717A
- Recall number
- Z-0321-06
- Recalling firm
- Philips Medical Systems
- Product
- HeartStart Pads Pediatric Plus, Pediatric Plus Multifunction Defibrillation Electrode Pads Model M3717A
- Status
- Terminated
- Initiated
- 2005-11-18
- Posted
- 2005-12-23
- Terminated
- 2006-07-12
- Reason
- The Apex/Anterior and the Sternum/Posterior pad labels are located in reverse position to the wire and connector
- Root cause
- Other
- Action
- Philips Medical sent the recall notification letter 11/30/05 via FedEx
- Quantity
- 253 CASES (5/CS)
- Distribution
- Nationwide Foreign: Australia, Canada, France, germany, Spain,, Sweden, Switzerland, UK
- Lot, serial or model codes
- Lot Number : Y042005-1
- 510(k) numbers
- ["K003228"]
- PMA numbers
- not on file
- Product code
- MLN
- Firm FEI
- 1218950
- Firm city
- Andover
- Firm state
- MA
- 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