FDA Medical Device Recalls (openFDA)
Gillette Research Institute: CrossAction Power Brushead Refills, Soft 2-Count Pack NDC:0-69055-82663-8
- Recall number
- Z-0184-05
- Recalling firm
- Gillette Research Institute
- Product
- CrossAction Power Brushead Refills, Soft 2-Count Pack NDC:0-69055-82663-8
- Status
- Terminated
- Initiated
- 2004-10-27
- Posted
- 2004-11-06
- Terminated
- 2005-11-21
- Reason
- Brushhead may unlatch from the power handle
- 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.
- Quantity
- not on file
- Distribution
- Nationwide
- Lot, serial or model codes
- All
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- JEQ
- Firm FEI
- 1000496207
- Firm city
- Needham
- Firm state
- MA
- 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
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
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