FDA Medical Device Recalls (openFDA)
Proctor & Gamble Co: The product is refill heads for battery powered toothbrushes. Spinbrush Pro Whitening Medium Refills, UPC 7 66878 00194 4.
- Recall number
- Z-0378-05
- Recalling firm
- Proctor & Gamble Co
- Product
- The product is refill heads for battery powered toothbrushes. Spinbrush Pro Whitening Medium Refills, UPC 7 66878 00194 4.
- Status
- Terminated
- Initiated
- 2004-11-11
- Posted
- 2004-12-30
- Terminated
- 2012-04-12
- Reason
- Market withdrawal of Crest Spinbrush Pro-Whitening. The firm has determined that there is a quality issue in certain production that may allow the circular brush at the tip of the brush head to become detached over time in a very small number of brushes.
- Root cause
- Other
- Action
- The firm notified distributors by letter on November 11, 2004. Distributors are asked to contact all of their retail stores.
- Quantity
- 7.5 million toothbrushes and refill heads.
- Distribution
- Nationwide
- 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