Becton Dickinson & Company BD Bard-Parker Special Surgeon''s Peridontia Blade, Sterile, Single Use Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
BD Bard-Parker Special Surgeon''s Peridontia Blade, Sterile, Single Use
Brand
Becton Dickinson & Company
Lot Codes / Batch Numbers
Lot # 4174460, Reorder # 371712
Products Sold
Lot # 4174460, Reorder # 371712
Becton Dickinson & Company is recalling BD Bard-Parker Special Surgeon''s Peridontia Blade, Sterile, Single Use due to BD received reports of unit packages labeled with the incorrect blade edge. The incorrectly labeled unit packages indicate a '12' (single edged blade). Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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).
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026