Z-0830-04

ABG Replacement Pump Assembly Catalog Number: 37092

Name: Z-0830-04 ABG Replacement Pump Assembly Catalog Number: 37092
Creator: Nova Biomedical Corporation
Published: 2004-03-30
License: https://open.fda.gov/license/

Nova Biomedical Corporation / initiated 2004-03-30 / Terminated / root cause: manufacturing process

FDA source

Nova Biomedical Corporation began a recall of ABG Replacement Pump Assembly Catalog Number: 37092 on 2004-03-30. The reason FDA records is "Incorrectly assembled pumps may result in inconsistent compression of the tubing causing erratic results or calibration problems". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-0830-04
Status: Terminated
Initiated: 2004-03-30
Posted: 2004-07-20
Terminated: 2004-06-17
Recalling firm: Nova Biomedical Corporation
Product: ABG Replacement Pump Assembly Catalog Number: 37092
Product code: CHL Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph
Reason for recall: Incorrectly assembled pumps may result in inconsistent compression of the tubing causing erratic results or calibration problems
Root cause tag: manufacturing process
FDA root cause: Other
Action: Nova Biomedical notified users by telephone on 3/31/04 and conducted follow-up by letter either by email or fax. On-site visit will be scheduled to replace the pump assembly.
Quantity in commerce: 5 units
Distribution: CA, IL, LA, MA ,NJ, NY, OH, PA, TX International: Italy ,England, Japan,Turkey., U.A.E., Greece, Thailand, Switzerland, Finland, Saudi Arabia, Italy, Mexico, Trinidad, Ireland, France, Cyprus, Czech Republic, ,Germany
Product codes and lots: Devices shipped between March 30-31, 2004

Product code CHL

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)