Z-0856-2007

Precision Xtra Blood Glucose monitoring system. Individual test meter and test strip kit

Name: Z-0856-2007 Precision Xtra Blood Glucose monitoring system. Individual test meter and test strip kit
Creator: Abbott Diabetes Care, Inc.
Published: 2007-03-05
License: https://open.fda.gov/license/

Abbott Medical / initiated 2007-03-05 / Terminated

FDA source

Abbott Diabetes Care, Inc. began a recall of Precision Xtra Blood Glucose monitoring system. Individual test meter and test strip kit on 2007-03-05. The reason FDA records is "The front button covers may detach from the meter". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0856-2007
Status: Terminated
Initiated: 2007-03-05
Posted: 2007-06-07
Terminated: 2008-04-04
Recalling firm: Abbott Medical
Product: Precision Xtra Blood Glucose monitoring system. Individual test meter and test strip kit.
Product code: NBW System, Test, Blood Glucose, Over The Counter
Reason for recall: The front button covers may detach from the meter.
FDA root cause: Other
Action: The firm intends to send letters to all customers that have registered their units under the firm's warranty database and the firm's first consignees. In addition, this notification will be placed on the company website, with e-mail and phone contacts as needed. Letter dated March 5, 2007.
Quantity in commerce: approximately 300 lots
Distribution: Product was distributed worldwide.
Product codes and lots: Other Brand names include: Precision Xceed Blood Glucose Monitoring system, Optium Xceed, Omron, HEA-214, Optium Xido, MediSense Optium, Boots, Optium (includes Medline and Liberty), Kroger, ReliOn, Rite Aid.

Product code NBW

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)