BEUDAMED
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    Synthes(R) Hemostatic Bone Putty, Part numbers 08.901.001.97S, 08.901.001.98S, 08.901.001.99S, 08.901.001D, and VB1025.10S. Indicated for use as a water soluble implant material and for use in the control of bleeding from bone surfaces.

    FDA Recall
    Terminated ·Synthes USA HQ, Inc.·Product code MTJ·July 5, 2012

    Hemostatic Bone Putty, for use as a water-soluble implant material and for use in the control of bleeding from bone surfaces.

    FDA Recall
    Terminated ·Synthes, Inc.·Product code MTJ·January 6, 2012

    Bone Wax. Ethicon, Inc. Bone wax is available sterile in individual foil envelopes, each containing 2.5 grams, and then packaged in an individually sealed over wrap packet. The device is indicated for use to control bleeding from the bone surface during surgical procedures.

    FDA Recall
    Terminated ·Ethicon, Inc. US·Product code MTJ·October 28, 2008

    Titanium MPJ (Toe Implant)TOE JOINT TITANIUM NPC LG, Part ID 16816

    FDA Enforcement
    Class II ·Terminated·BioPro, Inc.·March 9, 2022

    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC LG, Part ID 17038

    FDA Enforcement
    Class II ·Terminated·BioPro, Inc.·March 9, 2022

    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MS, Part ID 17197

    FDA Enforcement
    Class II ·Terminated·BioPro, Inc.·March 9, 2022

    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC ML, Part ID 16815

    FDA Enforcement
    Class II ·Terminated·BioPro, Inc.·March 9, 2022

    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MD, Part ID 17036

    FDA Enforcement
    Class II ·Terminated·BioPro, Inc.·March 9, 2022

    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC SM, Part ID 16813

    FDA Enforcement
    Class II ·Terminated·BioPro, Inc.·March 9, 2022

    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MS, Part ID 17198

    FDA Enforcement
    Class II ·Terminated·BioPro, Inc.·March 9, 2022

    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MD, Part ID 16814

    FDA Enforcement
    Class II ·Terminated·BioPro, Inc.·March 9, 2022

    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC M/L, Part ID 17037

    FDA Enforcement
    Class II ·Terminated·BioPro, Inc.·March 9, 2022

    Titanium MPJ (Toe Implant)TOE JOINT TITANIUM PC SM, Part ID 17035

    FDA Enforcement
    Class II ·Terminated·BioPro, Inc.·March 9, 2022

    MAJ-247 SINGLE USE 30MM REPLACEMENT BASKET, model no. MAJ-247 - Product Usage: REPLACEMENT BASKET for BML-3Q Mechanical Lithotripter.

    FDA Recall
    Terminated ·Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan·Product code LQC·January 4, 2021

    MAJ-244 SINGLE USE 30MM REPLACEMENT BASKET, model no. MAJ-244 - Product Usage: REPLACEMENT BASKET for BML-3Q Mechanical Lithotripter.

    FDA Recall
    Terminated ·Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan·Product code LQC·January 4, 2021

    MAJ-247 SINGLE USE 30MM REPLACEMENT BASKET, model no. MAJ-247 - Product Usage: REPLACEMENT BASKET for BML-3Q Mechanical Lithotripter.

    FDA Enforcement
    Class II ·Terminated·Aomori Olympus Co., Ltd.·February 17, 2021

    MAJ-244 SINGLE USE 30MM REPLACEMENT BASKET, model no. MAJ-244 - Product Usage: REPLACEMENT BASKET for BML-3Q Mechanical Lithotripter.

    FDA Enforcement
    Class II ·Terminated·Aomori Olympus Co., Ltd.·February 17, 2021

    Olympus MAJ-209 Single Use Suction Valves, Model Number MAJ-209 Product Usage: This product has been designed to be attached to the suction cylinder of compatible endoscopes for aspirating fluid from the distal end of the endoscopes through the instrument channel. Compatible endoscopes include Olympus bronchoscopes, cystoscopes, rhino-laryngoscopes and pleurascopes models.

    FDA Enforcement
    Class II ·Terminated·Olympus Corporation of the Americas·August 14, 2019

    Olympus MAJ-209 Single Use Suction Valves, Model Number MAJ-209 Product Usage: This product has been designed to be attached to the suction cylinder of compatible endoscopes for aspirating fluid from the distal end of the endoscopes through the instrument channel. Compatible endoscopes include Olympus bronchoscopes, cystoscopes, rhino-laryngoscopes and pleurascopes models.

    FDA Recall
    Terminated ·Olympus Corporation of the Americas·Product code EOQ·April 1, 2019

    Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm, Model. No. MAJ-1664

    FDA Recall
    Terminated ·Olympus Corporation of the Americas·Product code FEM·June 10, 2019