Z-0145-04

Portable Oxygen Analyzer

Name: Z-0145-04 Portable Oxygen Analyzer
Creator: Teledyne Analytical Instruments
Published: 2003-10-27
License: https://open.fda.gov/license/

Teledyne Analytical Instruments / initiated 2003-10-27 / Terminated

FDA source

Teledyne Analytical Instruments began a recall of Portable Oxygen Analyzer on 2003-10-27. The reason FDA records is "Potential failure to display the battery low light to the end-user". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0145-04
Status: Terminated
Initiated: 2003-10-27
Posted: 2004-07-20
Terminated: 2004-02-20
Recalling firm: Teledyne Analytical Instruments
Product: Portable Oxygen Analyzer
Product code: CCL Analyzer, Gas, Oxygen, Gaseous-Phase
Reason for recall: Potential failure to display the battery low light to the end-user.
FDA root cause: Other
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.
Quantity in commerce: 170
Distribution: FL, CA, UT, AZ and MO. New Zealand, Australia, Canada and the United Kingdom
Product codes and lots: Model AX300, Model MX300

Product code CCL

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)