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Terminated

AG-920RA Multi-gas unit analyzer

FDA Recall Z-0506-04 · Posted 2004-01-31

Recalling FirmNihon Kohden America Inc
Recall StatusTerminated
Product CodeCCK
Date Initiated2003-12-05
Date Terminated2004-02-17
Product Quantity24

Reason for Recall

Manufacturing error results in screw affecting electromagnetic interferences. Also metal lid is not tight enough.

Firm Action

Consignees were notified on 12/5/03. All have received return authorizations.

Root Cause

Other

Distribution Pattern

CA, OK, NV

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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