183 results · 24ms · Sources: EU EUDAMED, US FDA

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Legend Lubricant System (Legend Gold, Gold Touch and Platinum motors and Legend Lubricant/Diffuser cartridge)

FDA Recall
Terminated ·Medtronics Midas Rex·Product code HBB·November 11, 2002

Medtronic Midas Rex Legend High Speed Pneumatic System

FDA Recall
Terminated ·Power Surgical Solutions·Product code HBB·November 11, 2004

Tool Legend 16cm 2.4 mm wire pass for Midas Rex Legend Dissecting Tool. Used by surgeons to drill holes.

FDA Recall
Terminated ·Medtronic Sofamor Danek Usa, Inc Dallas Distribution·Product code HBB·October 21, 2015

Medtronic Midas Rex Classic, GS and Legend dissecting tools manufactured by Medtronic Inc. Powered Surgical Solutions, 4620 North Beach Street, Fort Worth, tX 76137 USA, Rx only, Sterile, Single Use Only.

FDA Recall
Terminated ·Power Surgical Solutions·Product code GET·September 1, 2005

Medtronic Midas Rex Dissecting Tool Legend 10 cm 4mm BA DIAM. Intended for use in neurosurgery.

FDA Recall
Terminated ·Medtronic Sofamor Danek Usa, Inc Dallas Distribution·Product code HBB·April 8, 2016

Medtronic MIDAS REX Legend High Speed Pneumatic System, Gold Touch Motor. Manufactured by Medtronic, Inc. Powered Surgical Solutions, 4620 North Beach Street, Fort Worth, TX 76137.

FDA Recall
Terminated ·Medtronic Powered Surgical Solutions·Product code HBB·June 29, 2005

Medtronic Midas Rex Legacy Telescoping Dissection Tool, Model TDQ-130D, manufactured by Medtronic Powered Surgical Solutions, Fort Worth, Texas 76137

FDA Recall
Terminated ·Power Surgical Solutions·Product code GET·January 3, 2005

Medtronic Midas Rex Legend Lubricant/ Diffuser Cartridge Catalog number PA100-A, manufactured by Medtronic Powered Surgical Solutions, Fort Worth, Texas

FDA Recall
Terminated ·Power Surgical Solutions·Product code HBB·November 3, 2004

UltraStream Exchange Kit Model Numbers 32001524 (24 cm), 32001528 (28cm), 32001532 (32 cm), and 32001536 (36 cm) and 32002540 (40 cm). The Rex Medical UltraStream Chronic Hemodialysis Catheter is a chronic hemodialysis catheter that can achieve high flow rates at low arterial pressures.

FDA Recall
Terminated ·Argon Medical Devices, Inc·Product code MSD·June 5, 2014

UltraStream Peel Away Kit; Model Numbers 32401524 (24 cm), 32401528 (28cm), 32401532 (32 cm), and 32401536 (36 cm) and 32402540 (40 cm) The Rex Medical UltraStream Chronic Hemodialysis Catheter is a chronic hemodialysis catheter that can achieve high flow rates at low arterial pressure.

FDA Recall
Terminated ·Argon Medical Devices, Inc·Product code MSD·June 5, 2014

UltraStream Chronic Hemodialysis Catheter Standard Kit; Model Number 32101524 (24 cm), 32101528 (28cm), 32101532 (32 cm), and 32101536 (36 cm) and 32102540 (40 cm). The Rex Medical UltraStream Chronic Hemodialysis Catheter is a chronic hemodialysis catheter that can achieve high flow rates at low arterial pressure.

FDA Recall
Terminated ·Argon Medical Devices, Inc·Product code MSD·June 5, 2014

Medtronic Midas Rex Legend Footed Attachment, AF01. Intended for use with all Legend and Legend EHS motors for general surgery including maxillofacial , craniofacial and sternotomy applications.

FDA Recall
Terminated ·Medtronic Sofamor Danek Usa, Inc Dallas Distribution·Product code HBB·November 30, 2009

Medtronic Midas Rex Legend tapered dissecting tool, Model F2/8TA23 Medtronic Powered Surgical Solutions, Forth Worth, TX Intended for use in Spinal, Cranial, Orthopedic, General Surgical and Plastic Surgery applications for transection, osteotomy, graft harvesting, bone shaping, laminectomy, entry hole, suture hole, and midface advancement.

FDA Recall
Terminated ·Medtronic Powered Surgical Solutions·Product code HBB·May 30, 2008

Lockheed Martin Gyrocam Systems ( LMGS) LMGS 15" camera systems. Laser pointer and illuminator used for law enforcement surveillance from aircraft. Models DNV, TS and DS

FDA Recall
Terminated ·Lockheed Martin Gyrocam Systems, Inc.·Product code REX·January 21, 2010

- Cannulated Drill Bit for Mini TightRope Ref. AR-8911DC Lot 122511 - Drill Bit, Straight Shank 2.7mm x 12.7cm Ref. 2318-027-00 Lot 122322 - Drill Bit, w/Depth Mark, Quick Coupling (Red) 2.0mm x 140mm Ref. 323.062 Lot 122347 - Fast Cutting Drill Bit 2.0mm Ref. FDB 2.0 Lot 122289, 122322 - Midas Rex Metal Cutting Drill Bit 3.0mm x 18.3mm Ref. MC30 Lot 122347 Orthopedic manual surgical instrument

FDA Recall
Terminated ·Surgical Instrument Service And Savings, Inc.·Product code HTW·May 3, 2013

Varian brand Clinac C-series Pendant Radiation delivery system. All model numbers included. Model numbers 2100, 2100C/D, 21 EX. 2300 C/D, 23 EX, 600C, 600 C/D, 2500 C, Trilogy, 6EX and Silhouette.

FDA Recall
Terminated ·Varian Medical Systems Inc·Product code IYE·June 6, 2006

PRO-DEX Surgical Driver Battery Pack PDBP-001 Series PRO-DEX Battery Pack, Single Pouch - PDBP-001-2 PRO-DEX Battery Pack, 40 Pouches - PDBP-040-2 Product Usage: -The PDBP-001 Battery is a single use (non-rechargeable) sterile lithium ion battery accessory that powers the PDSD Surgical driver. There is only one PDSD Surgical driver currently being produced (PDSD-5000) and the battery only works to power this driver. -The PDSD Series surgical drivers are Pro-Dex Branded surgical fixation drivers meant to drive surgical screws into bone in the CMF region of the body. They are class I exempt (Product codes GEY/GXL) battery powered hand pieces with a fixed collet. The only accessory is the PDBP-001 battery.

FDA Recall
Terminated ·Pro-Dex Inc·Product code GEY·September 25, 2018

Battery Pack KLS-SD-1000 Case (40 ct) Models: KLS-BP-040 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).

FDA Recall
Terminated ·Pro-Dex Inc·Product code MOQ·December 23, 2015

Battery Pack KLS-SD-1000 Single Models: KLS-BP-001 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).

FDA Recall
Terminated ·Pro-Dex Inc·Product code MOQ·December 23, 2015

Bard DuaLok Breast Lesion Localization Wire, Product Code (Gauge x Length) LW0037 (20gx37mm); LW0057 (20gx57mm), LW0077(20gx77mm), LW0107(20gx107mm), LW0137(20gx137mm). The Bard DuaLok Breast Lesion Localization Wire is intended for use as a guide for directing surgical biopsies.

FDA Recall
Terminated ·Bard Peripheral Vascular Inc·Product code GDF·August 26, 2014