Z-0779-05

Cidexplus Solution Test Strips

Name: Z-0779-05 Cidexplus Solution Test Strips
Creator: Advanced Sterilization Products
Published: 2005-03-16
License: https://open.fda.gov/license/

Advanced Sterilization Products / initiated 2005-03-16 / Terminated

FDA source

Advanced Sterilization Products began a recall of Cidexplus Solution Test Strips on 2005-03-16. The reason FDA records is "CIDEX test strips were found to pass solution below MEC". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0779-05
Status: Terminated
Initiated: 2005-03-16
Posted: 2005-04-27
Terminated: 2007-03-20
Recalling firm: Advanced Sterilization Products
Product: Cidexplus Solution Test Strips
Product code: JOJ Indicator, Physical/Chemical Sterilization Process
Reason for recall: CIDEX test strips were found to pass solution below MEC.
FDA root cause: Other
Action: Customers were notified via urgent product recall letter dated March 16, 2005, to return the product for replacement.
Quantity in commerce: 3422 cases (2 bottles per case)
Distribution: Nationwide & Puerto Rice
Product codes and lots: Product Code: 2924 Lot Numbers: 011480, 011483, 011019 Product Code: 2926 Lot Numbers: 011283, 011020

Product code JOJ

K981054Class IIBrowne Ga Indicator for Cidex ProductsAlbert Browne , Ltd. / cleared 1998-12-07

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)