Z-0596-04

MediSense Precision QID Blood Glucose Test Strips. The product is sold in box of 50 and 100. The NDC number...

Name: Z-0596-04 MediSense Precision QID Blood Glucose Test Strips. The product is sold in box of 50 and 100. The NDC number...
Creator: AmeriSource Bergen
Published: 2004-01-30
License: https://open.fda.gov/license/

AmeriSource Bergen / initiated 2004-01-30 / Terminated

FDA source

AmeriSource Bergen began a recall of MediSense Precision QID Blood Glucose Test Strips. The product is sold in box of 50 and 100. The NDC number for the 50 count box is 57599-7400-4. The NDC... on 2004-01-30. The reason FDA records is "potential counterfeit product/box". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0596-04
Status: Terminated
Initiated: 2004-01-30
Posted: 2004-07-20
Terminated: 2005-05-16
Recalling firm: AmeriSource Bergen
Product: MediSense Precision QID Blood Glucose Test Strips. The product is sold in box of 50 and 100. The NDC number for the 50 count box is 57599-7400-4. The NDC number for the 100 count box is 57599-7401-5.
Product code: CGA Glucose Oxidase, Glucose
Reason for recall: potential counterfeit product/box
FDA root cause: Other
Action: The recalling firm issued a recall letter to their direct accounts informing them of the problem and the need to return the product.
Quantity in commerce: unknown
Distribution: The products were shipped to retail and hospital pharmacies nationwide, Puerto Rico and the Bahamas.
Product codes and lots: Lot number 89873 exp 4/30/04, Lot number 90524 exp. 11/30/04, Lot number 90848 exp. 1/31/05, Lot number 90891 exp. 1/31/05, and Lot number 91326 exp. 3/31/05.

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)