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    T.S. MEDICAL CIRCUMCISION CLAMP

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Excalibur Introducer System

    FDA UDI
    Bard Access Systems, Inc.·00801741074769·EXCALIBUR INTRO 3FR

    Baltic Denture System BDLoad

    FDA UDI
    Merz Dental GmbH·D7091033403·Baltic Denture System BDLoad BDLoad ↓ Mn6 PLSEu...

    Cardiovascular Procedure Kit

    FDA UDI
    Terumo Cardiovascular Systems Corporation·00699753461581·

    ENDOSCOPIC MONOPOLAREECTRODE, MODEL EME- 1000 TO 1999

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    TRI-FIX SPINAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SMART MONITOR 2 PS

    FDA Adverse Event
    Malfunction ·PHILIPS RESPIRONICS -CHMV·Product code NPF·August 26, 2014

    ABRAMS MULTIDENSITY POLYURETHAN FOAM WOUND DRESSING SYSTEM

    FDA Adverse Event
    Other ·DR LEN'S MEDICAL PRODUCTS·Product code FRO·October 11, 2005

    CARDIOVASCULAR PROCEDURE KIT

    FDA Adverse Event
    Injury ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code OEZ·May 9, 2013

    TABS

    FDA Adverse Event
    Malfunction ·STANLEY SECURITY SOLUTIONS, INC·Product code KMI·February 20, 2013

    AVAULTA SOLO SYNTHETIC SUPPORT SYSTEM

    FDA Adverse Event
    Injury ·C.R. BARD, INC.·Product code FTL·March 24, 2011

    HEPARIN I.V. FLUSH SYRINGE, 100 UNITS/ML

    FDA Adverse Event
    Injury ·MEDEFIL·Product code NZW·April 23, 2008

    SMART MONITOR 2 PS

    FDA Adverse Event
    Malfunction ·PHILIPS RESPIRONICS - CHMV·Product code NPF·May 30, 2013

    Cardiovascular Procedure Kit containing Disposable Centrifugal Pumphead with or without X-Coating, sterile single use. Catalog numbers 73431, 73813-03, 74277, 72481-01, 72427, 70947-03, 74570-01, 74031-01, 73312-01, 74362, 74928, 74928-01, 72997-03, 74277, 70334-03, 73230, 73728, 71537, 73605-01, 74482-01, 74857-01, 74916, 73928-02, 70123-02, 71853-02, 72997-03, 74766, 71537, 73728, 72269, 74466, 71317-02 72991-02, 74951, 74336, 74121-01, 72941-01, 73315-03, 74559, 74277, 71382-01, 73108-02, 74178-03, 71598-02, 73108-02, 74618-01, 70334-03, 74802-01, 74916, 71932-02, 70951-03, 73957-01, 74857-01, 70957-02, 73449-01, 73124, 71546-02, 72892-01, 74431, 72370, 73913-01, 73957-01, 75028, 71820-01, 74201, 74402, 73891-01, 73865, 73972, 71175-01, 73208-03, 72669-02, 70533-09, 72275-01, 74369, 74321-01, 73175, B73235, 74459, 73931, 74262-01, 71002-01, 74879-01, 71801-01, 72384, 74365, 74366, 74348-01, 72072-02, 74048, 70932-03, 73407, 74879-01, 73820-01, 74161-01, 72991-02, 73288-01, 70016, 70466-08, 70188-04, 72238-02, 72817-01, 71103-02, 71717-01, 70957-02, 70196-02, 73872-02, 71896-02, 73191-01, 70977-05, 73438, 73201-01, 74671, 70367-07, 73276-02, 74482-01, 73551-02, 71537, 74348-01, 73211-01, 74430, 72026-03, 74502, 74873, 73652-01, 74163-02, 71733-02, 70075-06, 72846, 73820-01, 75063, 74155-01, 74454-01, 73428-01, 73442-01, 70664-01, 70012-05, 70099-03, 70159-05, 70917, 72965-02, 73645-01, 74417, 73346, 74433, 74737, 73055-02, 70227-04, 70880-05, 71934-02, 72073-01, 72149-01, 74120-01, 72370, 73662-03, 74251, 73872-02, 70658-09, 74550, 74124, 74096-01, 74203, 70174-09, 71485-01, 71905-01, 73124, 73874, 74467-01, 8327TXC-08, 8365TXC-01, 8390TXC, 74433, and 74737. For use only in the extracorporeal circuit for the cardiopulmonary bypass procedures.

    FDA Enforcement
    Class II ·Terminated·Terumo Cardiovascular Systems Corporation·July 23, 2014

    Cardiovascular Procedure Kit containing Disposable Centrifugal Pumphead with or without X-Coating, sterile single use. Catalog numbers 73431, 73813-03, 74277, 72481-01, 72427, 70947-03, 74570-01, 74031-01, 73312-01, 74362, 74928, 74928-01, 72997-03, 74277, 70334-03, 73230, 73728, 71537, 73605-01, 74482-01, 74857-01, 74916, 73928-02, 70123-02, 71853-02, 72997-03, 74766, 71537, 73728, 72269, 74466, 71317-02 72991-02, 74951, 74336, 74121-01, 72941-01, 73315-03, 74559, 74277, 71382-01, 73108-02, 74178-03, 71598-02, 73108-02, 74618-01, 70334-03, 74802-01, 74916, 71932-02, 70951-03, 73957-01, 74857-01, 70957-02, 73449-01, 73124, 71546-02, 72892-01, 74431, 72370, 73913-01, 73957-01, 75028, 71820-01, 74201, 74402, 73891-01, 73865, 73972, 71175-01, 73208-03, 72669-02, 70533-09, 72275-01, 74369, 74321-01, 73175, B73235, 74459, 73931, 74262-01, 71002-01, 74879-01, 71801-01, 72384, 74365, 74366, 74348-01, 72072-02, 74048, 70932-03, 73407, 74879-01, 73820-01, 74161-01, 72991-02, 73288-01, 70016, 70466-08, 70188-04, 72238-02, 72817-01, 71103-02, 71717-01, 70957-02, 70196-02, 73872-02, 71896-02, 73191-01, 70977-05, 73438, 73201-01, 74671, 70367-07, 73276-02, 74482-01, 73551-02, 71537, 74348-01, 73211-01, 74430, 72026-03, 74502, 74873, 73652-01, 74163-02, 71733-02, 70075-06, 72846, 73820-01, 75063, 74155-01, 74454-01, 73428-01, 73442-01, 70664-01, 70012-05, 70099-03, 70159-05, 70917, 72965-02, 73645-01, 74417, 73346, 74433, 74737, 73055-02, 70227-04, 70880-05, 71934-02, 72073-01, 72149-01, 74120-01, 72370, 73662-03, 74251, 73872-02, 70658-09, 74550, 74124, 74096-01, 74203, 70174-09, 71485-01, 71905-01, 73124, 73874, 74467-01, 8327TXC-08, 8365TXC-01, 8390TXC, 74433, and 74737. For use only in the extracorporeal circuit for the cardiopulmonary bypass procedures.

    FDA Recall
    Terminated ·Terumo Cardiovascular Systems Corporation·Product code KFM·April 14, 2014

    Presource Custom Sterile Surgical and Procedure Kits; general surgery trays; Cardinal Health, McGaw Park, IL 60085; The kit catalog numbers listed in the code information section below contain one or more of the following listed components for which Cardinal Health has been unable to confirm the manufacturer's compliance with section 502(o) of the FD&C Act: a) Split Dressing - 2"x 2", Yellow, component C-033-0022, vendor part number S1072; b) Tubing Extension Sets and IV Sets component C-FG711297CP, vendor pn FG711297CP; component C-FG711093CP, vendor pn FG711093CP; component C-FG711298CP, vendor pn FG711298CP; component C-FG711092CP, vendor pn FG711092CP; c) Cast Padding component C-9046, vendor pn 9046; component C-9044, vendor pn 9044; component C-9043, vendor pn 9043; component C-9062, vendor pn 9062; d) Scalpel Holder component C-DD1628-6, vendor pn DD1628-6; e) Latex Tubing component C-806-12, vendor pn 806-12; component C-808R, vendor pn 808R; component C-606R, vendor pn 606R; component C-122BA10, vendor pn 122BA10; component C-122BA12, vendor pn 122BA12; component C-122BA07, vendor pn 122BA07; component C-102BA12, vendor pn 102BA12; component C-099BA10, vendor pn 099BA10; component C-102BA10, vendor pn 102BA10; component C-103BA10, vendor pn 103BA10; component C-124BA10, vendor pn 124BA10; component C-140BA10, vendor pn 140BA10; f) Clinic Dropper component C-12548, vendor pn 10-871-00; g) Tongue Blade (depressor) component C-11820-010, vendor pn 07-920-00; h) Catheter Clamp component C-043-0497, vendor pn 033403-887; i) Gillette Good News Razor component C-P4417A, vendor pn 4417GN; j) Prepsicle Round Short Blue Swabstick component C-051-0401, vendor pn SBR20035; k) Tubing component C-SFM3-3050, vendor pn SFM3-3050; component C-SFM3-3650, vendor pn SFM3-3650; l) Specimen Container component C-B9021YN, vendor pn B9021YN; component C-C8846-18, vendor pn 15706-806; The kits are custom packed with all of the specific disposable class 1 and 2 devices required by the customer for specific types of surgery and medical procedures. These packs are then sterilized and are ready to be used by the customer for the specific procedure.

    FDA Recall
    Terminated ·Cardinal Health·Product code LRO·September 3, 2011

    Presource Custom Sterile Surgical and Procedure Kits; surgical trays; Cardinal Health, McGaw Park, IL 60085; The kit catalog numbers listed in the code information section below contain one or more of the following listed components for which Cardinal Health has been unable to confirm the manufacturer's compliance with section 502(o) of the FD&C Act: a) Split Dressing - 2"x 2", Yellow, component C-033-0022, vendor part number S1072; b) Tubing Extension Sets and IV Sets component C-FG711297CP, vendor pn FG711297CP; component C-FG711093CP, vendor pn FG711093CP; component C-FG711298CP, vendor pn FG711298CP; component C-FG711092CP, vendor pn FG711092CP; c) Cast Padding component C-9046, vendor pn 9046; component C-9044, vendor pn 9044; component C-9043, vendor pn 9043; component C-9062, vendor pn 9062; d) Scalpel Holder component C-DD1628-6, vendor pn DD1628-6; e) Latex Tubing component C-806-12, vendor pn 806-12; component C-808R, vendor pn 808R; component C-606R, vendor pn 606R; component C-122BA10, vendor pn 122BA10; component C-122BA12, vendor pn 122BA12; component C-122BA07, vendor pn 122BA07; component C-102BA12, vendor pn 102BA12; component C-099BA10, vendor pn 099BA10; component C-102BA10, vendor pn 102BA10; component C-103BA10, vendor pn 103BA10; component C-124BA10, vendor pn 124BA10; component C-140BA10, vendor pn 140BA10; f) Clinic Dropper component C-12548, vendor pn 10-871-00; g) Tongue Blade (depressor) component C-11820-010, vendor pn 07-920-00; h) Catheter Clamp component C-043-0497, vendor pn 033403-887; i) Gillette Good News Razor component C-P4417A, vendor pn 4417GN; j) Prepsicle Round Short Blue Swabstick component C-051-0401, vendor pn SBR20035; k) Tubing component C-SFM3-3050, vendor pn SFM3-3050; component C-SFM3-3650, vendor pn SFM3-3650; l) Specimen Container component C-B9021YN, vendor pn B9021YN; component C-C8846-18, vendor pn 15706-806; The kits are custom packed with all of the specific disposable class 1 and 2 devices required by the customer for specific types of surgery and medical procedures. These packs are then sterilized and are ready to be used by the customer for the specific procedure.

    FDA Recall
    Terminated ·Cardinal Health·Product code LRP·September 3, 2011

    Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

    FDA Enforcement
    Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012

    Smiths Medical Medfusion Model 4000 Syringe pump, Item Numbers: a) 4000-0101-249, b) 4000-0101-50, c) 4000-0101-51, d) 4000-0105-249, e) 4000-0105-50, f) 4000-0105-51, g) 4000-0105-78, h) 4000-0106-00, i) 4000-0106-01, j) 4000-0106-231,

    FDA Enforcement
    Class II ·Ongoing·Smiths Medical ASD Inc.·April 24, 2024

    Quadra Assura, Model No. CD3265-40, CD3265-40Q, CD3365-40C, CD3365-40Q. Quadra Assura MP, Model No. CD3269-40, CD3269-40Q, CD3369-40C. Fortify and Fortify Assura implantable cardioverter defibrillators (ICDS) are intended to provided ventricular anti-tachycardia pacing and ventricular defibrillation for automated treatment of life threatening ventricular arrhythmias. The devices may also be programmed to provide single or dual chamber bradycardia pacing. Unify and Unify Assura cardiac resynchronization therapy defibrillators (CRTDs) are intended to provide ventricular anti-tachycardia pacing and ventricular defibrillation for automated treatment of life-threatening ventricular arrhythmias. The devices may also be programmed to provide single or dual chamber bradycardia pacing, in additional to cardiac resynchronization therapy via left ventricular pacing

    FDA Enforcement
    Class I ·Terminated·St Jude Medical Inc.·November 2, 2016