Z-0560-06

BD Logic -- Blood Glucose Monitor

Name: Z-0560-06 BD Logic -- Blood Glucose Monitor
Creator: Becton Dickinson & Company
Published: 2006-01-05
License: https://open.fda.gov/license/

Becton Dickinson & Co / initiated 2006-01-05 / Terminated

FDA source

Becton Dickinson & Company began a recall of BD Logic -- Blood Glucose Monitor on 2006-01-05. The reason FDA records is "BD Blood Glucose Monitors may inadvertently switch the Unit of Measure from mg/dL to mmol/L or vice versa during battery insertion or when a meter is dropped". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0560-06
Status: Terminated
Initiated: 2006-01-05
Posted: 2006-02-25
Terminated: 2006-09-05
Recalling firm: Becton Dickinson & Co
Product: BD Logic -- Blood Glucose Monitor.
Product code: NBW System, Test, Blood Glucose, Over The Counter
Reason for recall: BD Blood Glucose Monitors may inadvertently switch the Unit of Measure from mg/dL to mmol/L or vice versa during battery insertion or when a meter is dropped.
FDA root cause: Other
Action: Recall notifications letters began mailing on 1/5/2006 to distributors, retailers, and DME providers. Healthcare professionals and consumers mailings will be during the week of 1/9/2006
Quantity in commerce: 840,808 units
Distribution: The firm distributes their blood glucose monitors Nationwide to distributors, retailers, durable Medical Equipment providers, Healthcare Professionals, and consumers. Foreign accounts include locations in Canada and Germany. There is one VA account.
Product codes and lots: All units under the following Catalog Number: 322051(48); 322029; 322068; 322069.

Product code NBW

K041478Class IIBd Logic Blood Glucose Monitor and Paradigm Link Blood Glucose MonitorBecton Dickinson / cleared 2004-10-28

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)