FDA Medical Device Recalls (openFDA)
Beckman Coulter Inc.: Access 2 Immunoassay System, Remanufactured, Catalog No. 386220 is an invitro diagnostic device used for the quantitative, semi-quantitative, or qualitative determination of various analytes concentrations found in human body fluids.
- Recall number
- Z-1956-2016
- Recalling firm
- Beckman Coulter Inc.
- Product
- Access 2 Immunoassay System, Remanufactured, Catalog No. 386220 is an invitro diagnostic device used for the quantitative, semi-quantitative, or qualitative determination of various analytes concentrations found in human body fluids.
- Status
- Terminated
- Initiated
- 2016-05-17
- Posted
- not on file
- Terminated
- 2016-08-26
- Reason
- Due to the lack of updated thermal components, these instruments may be more susceptible to the internal case temperature exceeding the 18 to 36 degrees Celsius operating range, causing SYS flags. The instrument will not report results until the internal case temperature returns to the operating range. This situation may cause a delay in the reporting of patient results.
- Root cause
- Under Investigation by firm
- Action
- An Urgent Medical Device Recall letter dated 5/17/16 was sent to customers to inform them that Beckman Coulter is recalling the Access 2 Immunoassay System, Remanufactured instrument, because it may not have all the updated thermal components installed. The letter informs customers of the impact and actions to be taken. The letter informs the customers that their Service Representative will contact them to schedule an onsite visit to inspect their instrument and update as needed. Customers are instructed to complete and return the enclosed Response Form within 10 days. Customers with any questions are instructed to contact Customer Technical Support Center: http://www.beckmancoulter.com, 1-800-854-3633 in the United States and Canada. Customers outside the United States and Canada are instructed to contact their local Beckman Coulter representative.
- Quantity
- 4 units total (1 unit in US)
- Distribution
- US, Morocco, Venezuela
- Lot, serial or model codes
- Serial No. 505143, 504805, 501368, 504231
- 510(k) numbers
- ["K922823"]
- PMA numbers
- not on file
- Product code
- JJE
- 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