FDA Device Intelligence
HomeDevice types › GES

Blade, Scalpel

FDA product code GES · Class 1 · General, Plastic Surgery

1,927
Registered devices
970
Adverse events
13
Recalls
48
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2022-10-27Southmedic, Inc.Upon review of its batch record, Southmedic identified that lot # W92761 was not sent out for sterilization, and was instead transferred directly to distributio
2016-06-27Aspen Surgical Puerto Rico Corp.After receiving a complaint the firm disclosed that Conventional Stainless Steel Surgical Blade catalog number 371712 lot 0088464 was incorrectly identified in
2012-08-15Surgical Specialties Puerto Rico Inc. dba Angiotech PR Inc.Potential for bent tips.
2012-08-15Surgical Specialties Puerto Rico Inc. dba Angiotech PR Inc.Potential for bent tips.
2012-08-15Surgical Specialties Puerto Rico Inc. dba Angiotech PR Inc.Potential for bent tips.
2012-08-15Surgical Specialties Puerto Rico Inc. dba Angiotech PR Inc.Potential for bent tips.
2009-09-29Merit Medical Systems, Inc.Potential sterility breach caused by excessive shipment damage.
2008-11-17Miltex, Inc.Blade may break: Over milling of the blade resulted in tip more narrow than specified.
2007-08-10Becton Dickinson & CompanyComplaints received of rust on the blades of BD Bard-Parker Surgical blades.
2007-08-10Becton Dickinson & CompanyComplaints received of rust on the blades of BD Bard-Parker Surgical blades.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.