FDA Medical Device Recalls (openFDA)
Cargille-Sacher Laboratories Inc.: Cargille Modified Kingsbury-Clark Albumin Standards For in vitro Diagnostics (Set of 8 Standards: 5, 10, 20, 30, 40, 50, 75, 100 mg/ml); Catalog number: 52064;
- Recall number
- Z-0479-2010
- Recalling firm
- Cargille-Sacher Laboratories Inc.
- Product
- Cargille Modified Kingsbury-Clark Albumin Standards For in vitro Diagnostics (Set of 8 Standards: 5, 10, 20, 30, 40, 50, 75, 100 mg/ml); Catalog number: 52064;
- Status
- Terminated
- Initiated
- 2006-07-07
- Posted
- 2009-12-01
- Terminated
- 2009-12-02
- Reason
- The 10 ml size standard of Cargille modified Kingsbury Clark Albumin Standards of lot Jan-12-05 appear shrunken or liquefied.
- Root cause
- Storage
- Action
- Cargill sent recall letters mailed July 7, 2006 by first class mail.
- Quantity
- 5 kits
- Distribution
- The product was distributed to 5 customers in OH, Washington, DC, PA, WI, and VA.
- Lot, serial or model codes
- Catalog number: 52064; Lot number: Jan-12-05
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- JIX
- Firm FEI
- 2210661
- Firm city
- Cedar Grove
- 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