FDA Medical Device Recalls (openFDA)
Excelsior Medical Corp: ESP 140 Syringe Pump. Used for medication infusion. Model 140A and 140D, manufactured by Excelsior Medical Corporation, Neptune, NJ.
- Recall number
- Z-0870-06
- Recalling firm
- Excelsior Medical Corp
- Product
- ESP 140 Syringe Pump. Used for medication infusion. Model 140A and 140D, manufactured by Excelsior Medical Corporation, Neptune, NJ.
- Status
- Terminated
- Initiated
- 2006-03-21
- Posted
- 2006-05-17
- Terminated
- 2006-12-07
- Reason
- Potential for alarm failure when the 140 pump completes infusion and/or the pump encounters a mid-infusion occlusion, when used in the 140 mode with a 140cc syringe. The ESP Pump works correctly when used in 60 mode with a 60cc syringe or smaller.
- Root cause
- Other
- Action
- An 'Urgent Recall' letter was mailed certified return receipt mail on 3/22/06 to all customers per distribution list.
- Quantity
- 3911 units
- Distribution
- Nationwide and Quebec, Canada
- Lot, serial or model codes
- All Serial Numbers since 1996.
- 510(k) numbers
- ["K914988"]
- PMA numbers
- not on file
- Product code
- FRN
- Firm FEI
- 1000122362
- Firm city
- Neptune
- Firm state
- NJ
- 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