Atlas FDA

AG-920RA Multi-gas unit analyzer

FDA device recall Z-0506-04 · posted 2004-01-31 · Terminated

Recall details

Recalling firm
Nihon Kohden America Inc
Reason for recall
Manufacturing error results in screw affecting electromagnetic interferences. Also metal lid is not tight enough.
Action taken
Consignees were notified on 12/5/03. All have received return authorizations.
Root cause
Other
Status
Terminated
Product code
CCK
Quantity affected
24
Distribution
CA, OK, NV
Date initiated
2003-12-05
Date posted
2004-01-31
Date terminated
2004-02-17
Location
Foothill Ranch, CA

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