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FDA Medical Device Recalls (openFDA)

Beckman Coulter Inc: Access and Access 2 Immunoassay Systems 862.2160 Discrete photometric chemistry analyzer for clinical use.

Recall number
Z-0619-03
Recalling firm
Beckman Coulter Inc
Product
Access and Access 2 Immunoassay Systems 862.2160 Discrete photometric chemistry analyzer for clinical use.
Status
Terminated
Initiated
2003-01-27
Posted
2003-03-06
Terminated
2003-10-08
Reason
Spring failure, design defect in component.
Root cause
Other
Action
A mandantory field modification was issued on 12/19/2002 to install the new spring on a next call basis unless a new spring was already installed (ie. recent purchase equipment)
Quantity
2418
Distribution
Product has been distributed in US from 8/92 to present. All these units are affected.
Lot, serial or model codes
Not applicable.
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

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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

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