Z-0266-2007

One Touch Basic/Profile and One Touch Ultra Blood Glucose Test Strips

Name: Z-0266-2007 One Touch Basic/Profile and One Touch Ultra Blood Glucose Test Strips
Creator: Core Care Technologies, Inc
Published: 2006-10-14
License: https://open.fda.gov/license/

Core Care Technologies, Inc / initiated 2006-10-14 / Terminated / root cause: manufacturing process

FDA source

Core Care Technologies, Inc began a recall of One Touch Basic/Profile and One Touch Ultra Blood Glucose Test Strips on 2006-10-14. The reason FDA records is "Counterfeit product (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-0266-2007
Status: Terminated
Initiated: 2006-10-14
Posted: 2007-01-05
Terminated: 2007-06-06
Recalling firm: Core Care Technologies, Inc
Product: One Touch Basic/Profile and One Touch Ultra Blood Glucose Test Strips
Product code: NBW System, Test, Blood Glucose, Over The Counter
Reason for recall: Counterfeit product (manufacturer unknown)
Root cause tag: manufacturing process
FDA root cause: Other
Action: The firm identified the customers who had been sent OneTouch test strips since August 2006 and contacted each by phone to identify the lot number of the test strips in the customer's possession. A letter was sent on 11/21/2006 by first class mail which identified the lot numbers identified in the letter from the law firm and providing instructions to follow if the affected lots were found.
Quantity in commerce: unknown
Distribution: Nationwide.
Product codes and lots: One Touch Basic/Profile Lot #''s 2606340, 2619932, 272894A, 2615211 One Touch Ultra Lot #''s 2691191, 2691261

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)