Z-0206-2007

One Touch Ultra Blood Glucose test strips, LifeScan, a Johnson & Johnson Co., 50 test strips, 2 vials of 25...

Name: Z-0206-2007 One Touch Ultra Blood Glucose test strips, LifeScan, a Johnson & Johnson Co., 50 test strips, 2 vials of 25...
Creator: Discount Diabetic Supply
Published: 2006-10-19
License: https://open.fda.gov/license/

Discount Diabetic Supply / initiated 2006-10-19 / Terminated / root cause: manufacturing process

FDA source

Discount Diabetic Supply began a recall of One Touch Ultra Blood Glucose test strips, LifeScan, a Johnson & Johnson Co., 50 test strips, 2 vials of 25 test strips on 2006-10-19. The reason FDA records is "Counterfeit-blood glucose 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-0206-2007
Status: Terminated
Initiated: 2006-10-19
Posted: 2007-01-05
Terminated: 2009-12-22
Recalling firm: Discount Diabetic Supply
Product: One Touch Ultra Blood Glucose test strips, LifeScan, a Johnson & Johnson Co., 50 test strips, 2 vials of 25 test strips
Product code: NBW System, Test, Blood Glucose, Over The Counter
Reason for recall: Counterfeit-blood glucose test strips (manufacturer unknown)
Root cause tag: manufacturing process
FDA root cause: Other
Action: The recalling firm notified its consignees of the problem and the recall by telephone on 10/19/2006. The firm followed this with a written notice on 10/30/2006.
Quantity in commerce: 240 units
Distribution: Nationwide distribution --- States of CA, TX, TN, GA, AL, and OK
Product codes and lots: Lot No. 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)