Z-0262-2007

One Touch Ultra Blood Glucose Test Strips

Name: Z-0262-2007 One Touch Ultra Blood Glucose Test Strips
Creator: Medical Plastics Devices Inc
Published: 2006-10-13
License: https://open.fda.gov/license/

Medical Plastics Devices Inc / initiated 2006-10-13 / Terminated / root cause: manufacturing process

FDA source

Medical Plastics Devices Inc began a recall of One Touch Ultra Blood Glucose Test Strips on 2006-10-13. The reason FDA records is "Counterfeit 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-0262-2007
Status: Terminated
Initiated: 2006-10-13
Posted: 2006-12-16
Terminated: 2007-07-24
Recalling firm: Medical Plastics Devices Inc
Product: One Touch Ultra Blood Glucose Test Strips
Product code: CGA Glucose Oxidase, Glucose
Reason for recall: Counterfeit Glucose Test Strips (manufacturer unknown)
Root cause tag: manufacturing process
FDA root cause: Other
Action: Medical Plastic Devices, Quebec, Canada notiifed customers by telephone on 10/17/06 and completed notification by letter on 10/18/06.
Quantity in commerce: 3,353 boxes (both Recall Z-0261 and Z-0262-2007)
Distribution: Nationwide
Product codes and lots: Lot Number: 2691191

Product code CGA

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)