Z-0185-05

CrossAction Power Brushead Refills, Medium 2-Count Pack NDC: 0-69055-82448-1

Name: Z-0185-05 CrossAction Power Brushead Refills, Medium 2-Count Pack NDC: 0-69055-82448-1
Creator: Gillette Research Institute
Published: 2004-10-27
License: https://open.fda.gov/license/

Gillette Research Institute / initiated 2004-10-27 / Terminated

FDA source

Gillette Research Institute began a recall of CrossAction Power Brushead Refills, Medium 2-Count Pack NDC: 0-69055-82448-1 on 2004-10-27. The reason FDA records is "Brushhead may unlatch from the power handle". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0185-05
Status: Terminated
Initiated: 2004-10-27
Posted: 2004-11-06
Terminated: 2005-11-21
Recalling firm: Gillette Research Institute
Product: CrossAction Power Brushead Refills, Medium 2-Count Pack NDC: 0-69055-82448-1
Product code: JEQ Toothbrush, Powered
Reason for recall: Brushhead may unlatch from the power handle
FDA root cause: Other
Action: Gillette issued recall notification letters on 10/27/04 via Fed''X to Distributors and retail accounts requesting the removal and return of the devices. In addtion a Consumer letter issued 10/27/04 to provide information to the special needs and others that they are offering a replacement product for those of special needs. Gillette will post the consumer notifcation on the Gillette (Gillette.com) and Oral-B (Oral-B.com) websites.
Distribution: Nationwide
Product codes and lots: All

Product code JEQ

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)