FDA Medical Device Recalls (openFDA)
I-Flow Corporation: Eclipse Infusion Pump, 250 ml X 250 ml per hour) Part 5001247
- Recall number
- Z-0312-04
- Recalling firm
- I-Flow Corporation
- Product
- Eclipse Infusion Pump, 250 ml X 250 ml per hour) Part 5001247
- Status
- Terminated
- Initiated
- 2002-08-19
- Posted
- 2004-01-09
- Terminated
- 2005-01-04
- Reason
- Slower than expected infusion of medications, such as antibiotics.
- Root cause
- Other
- Action
- All customers were contacted by telephone on 8/19/2002. Letters were also sent dated 8/27/2002. Recall is complete.
- Quantity
- 144
- Distribution
- not on file
- Lot, serial or model codes
- Lot 262073
- 510(k) numbers
- ["K020862"]
- PMA numbers
- not on file
- Product code
- MEB
- Firm FEI
- 3011270181
- Firm city
- Lake Forest
- Firm state
- CA
- 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