Z-0592-05

The product is refill heads for battery powered toothbrushes. Spinbrush Pro Whitening Medium Refill Heads...

Name: Z-0592-05 The product is refill heads for battery powered toothbrushes. Spinbrush Pro Whitening Medium Refill Heads...
Creator: Proctor & Gamble Co
Published: 2005-02-23
License: https://open.fda.gov/license/

The Procter & Gamble Co./THE GILLETTE Company / initiated 2005-02-23 / Terminated

FDA source

Proctor & Gamble Co began a recall of The product is refill heads for battery powered toothbrushes. Spinbrush Pro Whitening Medium Refill Heads, UPC776687800194 on 2005-02-23. The reason FDA records is "The brushes may experience head breakage when insufficently rinsed after use and when used in combination with toothpastes containing a combination baking soda, peroxide, and sodium lauroyl sarcosinate". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0592-05
Status: Terminated
Initiated: 2005-02-23
Posted: 2005-03-11
Terminated: 2006-04-13
Recalling firm: The Procter & Gamble Co./THE GILLETTE Company
Product: The product is refill heads for battery powered toothbrushes. Spinbrush Pro Whitening Medium Refill Heads, UPC776687800194.
Product code: JEQ Toothbrush, Powered
Reason for recall: The brushes may experience head breakage when insufficently rinsed after use and when used in combination with toothpastes containing a combination baking soda, peroxide, and sodium lauroyl sarcosinate.
FDA root cause: Other
Action: The recalling firm sent a recall letter dated 2/23/05 and dated 3/4/05.
Quantity in commerce: 15 million toothbrushes and refill heads
Product codes and lots: All codes.

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)