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Terminated

Portable Oxygen Analyzer

FDA Recall Z-0145-04 · Posted 2004-07-20

Recalling FirmTeledyne Analytical Instruments
Recall StatusTerminated
Product CodeCCL
Date Initiated2003-10-27
Date Terminated2004-02-20
Product Quantity170

Reason for Recall

Potential failure to display the battery low light to the end-user.

Firm Action

All affected customers will be notified by letter on 10/27/2003. All units returned will be reworked and 100% retested prior to shipment.

Root Cause

Other

Distribution Pattern

FL, CA, UT, AZ and MO. New Zealand, Australia, Canada and the United Kingdom

Official Source

View FDA Recall →

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

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