FDA Medical Device Recalls (openFDA)
Beckman Coulter Inc: Synchron Systems Lipid Calibrator (HDLD) Part 650218
- Recall number
- Z-1153-04
- Recalling firm
- Beckman Coulter Inc
- Product
- Synchron Systems Lipid Calibrator (HDLD) Part 650218
- Status
- Terminated
- Initiated
- 2003-10-03
- Posted
- 2004-07-23
- Terminated
- 2004-08-30
- Reason
- Incorrect units are printed in labeling but not in software.
- Root cause
- Other
- Action
- Letter was mailed which explains tha the units on the Value Sheet are printed incorrectly. Recall is complete.
- Quantity
- 2069
- Distribution
- Nationwide
- Lot, serial or model codes
- Kit; M302210 Level 1; M302211 Level 2; M302212
- 510(k) numbers
- ["K983640"]
- PMA numbers
- not on file
- Product code
- JIS
- Firm FEI
- 2050012
- Firm city
- Brea
- 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