Z-0477-2007

One Touch Ultra Blood Glucose Test Strips-Lot # 2691191, LifeScan

Name: Z-0477-2007 One Touch Ultra Blood Glucose Test Strips-Lot # 2691191, LifeScan
Creator: Matrix Distributors, Inc.
Published: 2006-10-09
License: https://open.fda.gov/license/

Matrix Distributors, Inc. / initiated 2006-10-09 / Terminated / root cause: manufacturing process

FDA source

Matrix Distributors, Inc. began a recall of One Touch Ultra Blood Glucose Test Strips-Lot # 2691191, LifeScan on 2006-10-09. The reason FDA records is "Counterfeit Test Strips (manufacturer unknown)". 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-0477-2007
Status: Terminated
Initiated: 2006-10-09
Posted: 2007-02-14
Terminated: 2008-01-07
Recalling firm: Matrix Distributors, Inc.
Product: One Touch Ultra Blood Glucose Test Strips-Lot # 2691191, LifeScan
Product code: NBW System, Test, Blood Glucose, Over The Counter
Reason for recall: Counterfeit Test Strips (manufacturer unknown)
Root cause tag: manufacturing process
FDA root cause: Other
Action: Matrix Distributors contacted by telephone those pharmacies to which they had shipped the affected lots. These call were conducted from 10/9 to 10/13/2006. A follow-up letter was issued to the pharmacies extending the recall to the user level.
Quantity in commerce: 800 units
Distribution: Product was distributed to 96 pharmacies throughout the United States.
Product codes and lots: One Touch Ultra Test Strips: Lot #'' 2691191.

Product code NBW

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)