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EZ-Blade Remover

DXM CO., LTD · Model EZ-Blade Remover · UDI-DI 08800017901688

GES

510(k) clearances

970

Adverse events

Recalls

304

Facilities

Description

Disposable Blade Remover is a simple but efficient way to prevent cuts, scrapes, and possible infection when removing and disposing blades with no direct contact with the blade Easily and securely remove used scalpel blades for disposal • Palm-sized round design made with rigid and durable polypropylene • User is able to safely and hygienically remove the blades with one simple pull • Store up to 100 blades • Store not only used scalpel blades but also medical needles, dermaplaning tools, dermaplaning razors, and other small blades

Recalls

Date	Firm	Reason
2022-10-27	Southmedic, Inc.	Upon review of its batch record, Southmedic identified that lot # W92761 was not sent out for sterilization, and was instead transferred directly to distribution where it was sold
2016-06-27	Aspen 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 the single unit foil
2012-08-15	Surgical Specialties Puerto Rico Inc. dba Angiotech PR Inc.	Potential for bent tips.
2012-08-15	Surgical Specialties Puerto Rico Inc. dba Angiotech PR Inc.	Potential for bent tips.
2012-08-15	Surgical Specialties Puerto Rico Inc. dba Angiotech PR Inc.	Potential for bent tips.
2012-08-15	Surgical Specialties Puerto Rico Inc. dba Angiotech PR Inc.	Potential for bent tips.
2009-09-29	Merit Medical Systems, Inc.	Potential sterility breach caused by excessive shipment damage.
2008-11-17	Miltex, Inc.	Blade may break: Over milling of the blade resulted in tip more narrow than specified.
2007-08-10	Becton Dickinson & Company	Complaints received of rust on the blades of BD Bard-Parker Surgical blades.
2007-08-10	Becton Dickinson & Company	Complaints received of rust on the blades of BD Bard-Parker Surgical blades.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.