BEUDAMED
    39 results · 12ms · Sources: EU EUDAMED, US FDA

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    OASIS Medical SOFT PLUG Extended Duration Plug, Reference 6403 (Lot LA1105E)

    FDA Recall
    Terminated ·Oasis Medical Inc·Product code LZU·July 6, 2006

    RUS Tool Version Software

    FDA Recall
    Terminated ·GE OEC Medical Systems, Inc·Product code JAA·August 16, 2006

    Product is 35mm Flex Tube***NON-STERILE PRODUCT***CAUTION: FEDERAL LAW RESTRICTS THIS DEVICE TO SALE BY OR ON THE ORDER OF A PHYSICIAN." W.LORENZ SURGICAL***WALTER LORENZ SURGICAL, INC. 1520 TRADEPORT DRIVE , REPLY TO POST OFFICE BOX 18009, JACKSONVILLE, FLORIDA 32229-8009 USA, 1-800-874-7711. Part # SP-1328-01 Lot 968720 Qty 34 10/6/2005. Sold for use with: Part # SP-1598-13 Lot # 041950 Qty 10. Part # SP-1597-13 Lot # 066720 Qty 9. Part # SP-1598-13 Lot 050140 Qty 15. Product Usage: Distraction devices are for use in bone stabilization and elongation (lengthening) when correction of oral, cranial, mandibular and maxiollofacial deficiencies or post traumatic defects require gradual bone distraction. Each implantable distraction device has a titanium alloy drive screw mechanism and LactoSorb resorbable correction plates, which are implanted by fixation with LactoSorb bone screws.

    FDA Recall
    Terminated ·Walter Lorenz Surgical, Inc.·Product code JEY·February 17, 2006

    GE OEC 9800 Fluoro C-Arm X-ray System, GE OEC Medical Systems Inc.

    FDA Recall
    Terminated ·GE OEC Medical Systems, Inc·Product code JAA·August 16, 2006

    GE OEC 9900 Elite Digital Mobile C-Arm X-ray system, GE OEC Medical Systems Inc.

    FDA Recall
    Terminated ·GE OEC Medical Systems, Inc·Product code JAA·August 16, 2006

    Product is 65mm Flexible Tube***NON-STERILE PRODUCT***CAUTION: FEDERAL LAW RESTRICTS THIS DEVICE TO SALE BY OR ON THE ORDER OF A PHYSICIAN." W.LORENZ SURGICAL***WALTER LORENZ SURGICAL, INC. 1520 TRADEPORT DRIVE , REPLY TO POST OFFICE BOX 18009, JACKSONVILLE, FLORIDA 32229-8009 USA, 1-800-874-7711. Part # 80-3112-01 Lot 976580 Qty 41 10/18/2005. Sold for use with: Part # 80-3112-01 Lot # 976580 Qty 28. Part # SP-1652 Lot # 048720 Qty 3. Part #-1640 Lot # 056620 Qty 8. Part # SP-1651 Lot # 056590 Qty 2. Part # 80-3112-01 Lot 970060 Qty 31 10/20/2005. Sold for use with: Part # SP-1651 Lot # 056590 Qty 8. Part # SP-1653 Lot # 056610 Qty 10. Part # SP-1285 Lot # 056570 Qty 4. Part # SP-1652 Lot # 056600 Qty 9. Product Usage: Distraction devices are for use in bone stabilization and elongation (lengthening) when correction of oral, cranial, mandibular and maxiollofacial deficiencies or post traumatic defects require gradual bone distraction. Each implantable distraction device has a titanium alloy drive screw mechanism and LactoSorb resorbable correction plates, which are implanted by fixation with LactoSorb bone screws.

    FDA Recall
    Terminated ·Walter Lorenz Surgical, Inc.·Product code JEY·February 17, 2006

    Product is 40mm Flexible Tube. ***NON-STERILE PRODUCT***CAUTION: FEDERAL LAW RESTRICTS THIS DEVICE TO SALE BY OR ON THE ORDER OF A PHYSICIAN." W.LORENZ SURGICAL***WALTER LORENZ SURGICAL, INC. 1520 TRADEPORT DRIVE , REPLY TO POST OFFICE BOX 18009, JACKSONVILLE, FLORIDA 32229-8009 USA, 1-800-874-7711. Part # 80-3111-01 Lot 052190 QTY 76 Pieces 10/18/2005. Sold for use with: Part # 80-3111-01 Lot 052190 Qty 14. Part # SP-1651 Lot # 069330 Qty 10. Part # SP-1639 Lot # 046230 Qty 4. Part # SP-1598-13 Lot # 041960 Qty 10. Part # SP-1329 Lot # 039700 Qty 10. Part # SP-1331 Lot # 039720 Qty 12. Part # SP-1330 Lot # 039710 Qty 11. Part # SP-1633 Lot # 056630 Qty 5. Product Usage: Distraction devices are for use in bone stabilization and elongation (lengthening) when correction of oral, cranial, mandibular and maxiollofacial deficiencies or post traumatic defects require gradual bone distraction. Each implantable distraction device has a titanium alloy drive screw mechanism and LactoSorb resorbable correction plates, which are implanted by fixation with LactoSorb bone screws.

    FDA Recall
    Terminated ·Walter Lorenz Surgical, Inc.·Product code JEY·February 17, 2006

    Kimberly Clark * Facet Block Tray * Single Use * Sterile * Rx only * Manufactured by Ballard Medical Products, Draper, Utah, 84020 USA * Distributed in the U.S. by Kimberly Clark Global States, Inc., Roswell, GA 30076, USA

    FDA Recall
    Terminated ·Kimberly-Clark Corporation·Product code CAZ·March 15, 2006

    Kimberly Clark * Universal Block Tray * Single Use * Sterile * Rx only * Manufactured by Ballard Medical Products, Draper, Utah, 84020 USA * Distributed in the U.S. by Kimberly Clark Global States, Inc., Roswell, GA 30076, USA

    FDA Recall
    Terminated ·Kimberly-Clark Corporation·Product code CAZ·March 15, 2006

    Kimberly Clark * Selective Nerve Block Tray * Single Use * Sterile * Rx only * Manufactured by Ballard Medical Products, Draper, Utah, 84020 USA * Distributed in the U.S. by Kimberly Clark Global States, Inc., Roswell, GA 30076, USA

    FDA Recall
    Terminated ·Kimberly-Clark Corporation·Product code CAZ·March 15, 2006

    Kimberly Clark * Nerve Block Tray * Single Use * Sterile * Rx only * Manufactured by Ballard Medical Products, Draper, Utah, 84020 USA * Distributed in the U.S. by Kimberly Clark Global States, Inc., Roswell, GA 30076, USA

    FDA Recall
    Terminated ·Kimberly-Clark Corporation·Product code CAZ·March 15, 2006

    Kimberly Clark * Nerve Root Block Tray * Single Use * Sterile * Rx only * Manufactured by Ballard Medical Products, Draper, Utah, 84020 USA * Distributed in the U.S. by Kimberly Clark Global States, Inc., Roswell, GA 30076, USA

    FDA Recall
    Terminated ·Kimberly-Clark Corporation·Product code CAZ·March 15, 2006

    Hitachi Echelon Magnetic Resonance Imaging System, Serial Number: V-001, equipped with CTL coil type: MR-CTL-150.

    FDA Recall
    Terminated ·Hitachi Medical Systems America Inc·Product code MOS·August 14, 2006

    Datex-Ohmeda Tec 6 Plus Desflurane Vaporizer. It is an electronic vaporizer which delivers the anesthetic agent desflurane.

    FDA Recall
    Terminated ·Datex Ohmeda, Inc·Product code CAD·September 15, 2006

    Kimberly Clark * 20' Minibore Extension Line * Single Use * Sterile * Rx only * Manufactured by Ballard Medical Products, Draper, Utah, 84020 USA * Distributed in the U.S. by Kimberly Clark Global States, Inc., Roswell, GA 30076, USA. This is a Pain Management Product that is sold in a wide variety of kits including both standard tray configurations and custom kits.

    FDA Recall
    Terminated ·Kimberly-Clark Corporation·Product code FPK·March 15, 2006

    AIRIS II, Altaire Nuclear Magnetic Resonance Imaging Device Systems

    FDA Recall
    Terminated ·Hitachi Medical Systems America Inc·Product code LNH·April 28, 2006

    Krystal Klear Rinse (China only)

    FDA Recall
    Terminated ·Advanced Medical Optics, Inc.·Product code LPN·September 15, 2006

    Complete Blink N Clean (US and Asia Pacific markets)

    FDA Recall
    Terminated ·Advanced Medical Optics, Inc.·Product code LPN·September 15, 2006

    COMPLETE MoisturePLUS Multi-Purpose Solution (US and Asia Pacific markets, excluding Japan) & COMPLETE Amino Moist Multi-Purpose Solution (Japan only)

    FDA Recall
    Terminated ·Advanced Medical Optics, Inc.·Product code LPN·September 15, 2006

    Lens Plus Ocupure Saline Sterile Rinsing Solution (Asia Pacific markets, excluding Japan) & Consept Rinsing Solution (Japan only)

    FDA Recall
    Terminated ·Advanced Medical Optics, Inc.·Product code LPN·September 15, 2006