Z-0403-03

Precision PCx Test Strips Part Number: 98757-12

Name: Z-0403-03 Precision PCx Test Strips Part Number: 98757-12
Creator: Abbott Laboratories, Inc.
Published: 2002-11-08
License: https://open.fda.gov/license/

Abbott Medical / initiated 2002-11-08 / Terminated

FDA source

Abbott Laboratories, Inc. began a recall of Precision PCx Test Strips Part Number: 98757-12 on 2002-11-08. The reason FDA records is "Use of glucose blood strips may provide false high results". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0403-03
Status: Terminated
Initiated: 2002-11-08
Posted: 2002-12-31
Terminated: 2017-02-13
Recalling firm: Abbott Medical
Product: Precision PCx Test Strips Part Number: 98757-12
Product code: CGA Glucose Oxidase, Glucose
Reason for recall: Use of glucose blood strips may provide false high results
FDA root cause: Other
Action: Abbott notified the two hospitals by telephone on 11/8/02. Both responded and returned product.
Quantity in commerce: 210 packages
Distribution: NC, WI
Product codes and lots: Lot Number: 146135

Product code CGA

K983504Class IIPrecision Xtra Advanced Diabetes Management System, Precision Blood Glucose Test Strips, Precision Xtra B-Ketone Test StMedisense, Inc. / cleared 1999-07-09

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)