FDA Medical Device Recalls (openFDA)
Becton Dickinson & Company: BD Bard-Parker Special Surgeon''s Peridontia Blade, Sterile, Single Use
- Recall number
- Z-0152-06
- Recalling firm
- Becton Dickinson & Company
- Product
- BD Bard-Parker Special Surgeon''s Peridontia Blade, Sterile, Single Use
- Status
- Terminated
- Initiated
- 2005-06-30
- Posted
- 2005-11-16
- Terminated
- 2007-02-01
- Reason
- BD received reports of unit packages labeled with the incorrect blade edge. The incorrectly labeled unit packages indicate a '12' (single edged blade) is present, the actual blade present is a '12B' (double edged blade).
- Root cause
- Other
- Action
- A urgent product recall was sent to distributors on 6/30/2005 by first class mail. End users were then identified and recall notifications were also sent to them. by first class mail.
- Quantity
- 11,900 units were distributed
- Distribution
- Product was distributed to 9 distributors nationwide and then to end users.
- Lot, serial or model codes
- Lot # 4174460, Reorder # 371712
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- GES
- Firm FEI
- 2243072
- Firm city
- Franklin Lakes
- Firm state
- NJ
- 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