FDA Medical Device Recalls (openFDA)
Proctor & Gamble Co: The product is a battery operated toothbrush. Spinbrush Pro Medium battery operated toothbrushes UPC 76687800079.
- Recall number
- Z-0594-05
- Recalling firm
- Proctor & Gamble Co
- Product
- The product is a battery operated toothbrush. Spinbrush Pro Medium battery operated toothbrushes UPC 76687800079.
- Status
- Terminated
- Initiated
- 2005-02-23
- Posted
- 2005-03-11
- Terminated
- 2006-04-13
- Reason
- 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.
- Root cause
- Other
- Action
- The recalling firm sent a recall letter dated 2/23/05 and dated 3/4/05.
- Quantity
- 15 million toothbrushes and refill heads
- Distribution
- not on file
- Lot, serial or model codes
- All codes.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- JEQ
- Firm FEI
- 1216894
- Firm city
- Cincinnati
- Firm state
- OH
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28