BEUDAMED
    32 results · 16ms · Sources: EU EUDAMED, US FDA

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

    FDA Recall
    Terminated ·BioPro, Inc.·Product code KWD·February 1, 2022

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

    FDA Recall
    Terminated ·BioPro, Inc.·Product code KWD·February 1, 2022

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

    FDA Recall
    Terminated ·BioPro, Inc.·Product code KWD·February 1, 2022

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

    FDA Recall
    Terminated ·BioPro, Inc.·Product code KWD·February 1, 2022

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

    FDA Recall
    Terminated ·BioPro, Inc.·Product code KWD·February 1, 2022

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

    FDA Recall
    Terminated ·BioPro, Inc.·Product code KWD·February 1, 2022

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

    FDA Recall
    Terminated ·BioPro, Inc.·Product code KWD·February 1, 2022

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

    FDA Recall
    Terminated ·BioPro, Inc.·Product code KWD·February 1, 2022

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

    FDA Recall
    Terminated ·BioPro, Inc.·Product code KWD·February 1, 2022

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

    FDA Recall
    Terminated ·BioPro, Inc.·Product code KWD·February 1, 2022

    Left Locking 2st MTP/MPJ Combo Fusion Plate. Product labeled in part, "ACUMED 5885 NW Cornelius pass Road Hillsboro, OR. 97124-9432... Size: Left Locking 2st MTP/MPJ Combo Fusion Plate... REF 70-0036-S... LOT W58123".

    FDA Recall
    Terminated ·Acumed LLC·Product code HWC·February 14, 2008

    Right Locking 1st MTP/MPJ Combo Fusion Plate. Product labeled in part, "ACUMED 5885 NW Cornelius pass Road Hillsboro, OR. 97124-9432... Size: Right Locking 1st MTP/MPJ Combo Fusion Plate... REF 70-0037-S... LOT W58148".

    FDA Recall
    Terminated ·Acumed LLC·Product code HWC·February 14, 2008

    Zimmer Gender Solution Patello-Femoral Joint (PFJ) System Patello-Femoral Trochlea Component, Precoat, Size 4, Left. Knee prosthesis.

    FDA Recall
    Terminated ·Zimmer, Inc.·Product code KRR·July 30, 2014

    Invacare Power Wheelchair, one per box To provide mobility to a person restricted to a sitting position.

    FDA Recall
    Terminated ·Invacare Corporation·Product code ITI·June 4, 2013

    CASMED 500cc Unifusor Classic with aneroid gauge and thumbwheel valve. Model: D803FGA. Private labeled for P.J. Dahlhausen in Germany. It is designed for use in rapid infusion,invasive pressure monitoring and with auto-transfusion devices.

    FDA Recall
    Terminated ·CAS Medical Systems, Inc.·Product code KZD·September 20, 2008

    KY SENSITIVE TM JELLY Personal Lubricant. The product is packaged into 3 oz tubes, which are then packed into a printed carton. Distributed by McNeil-PPC Inc.

    FDA Recall
    Terminated ·Mc-NEIL-PPC, Inc.·Product code NUC·January 25, 2013

    KY LIQUIBEADS Vaginal Moisturizer; Distributed By: McNeil-PPC, Inc. Skillman, NJ 08558-9418; UPC 380041087704; 380040087958. Personal lubricant

    FDA Recall
    Terminated ·Mc-NEIL-PPC, Inc.·Product code NUC·July 2, 2012

    KY SilkE Vaginal Moisturizer and Personal Lubricant. The product is packaged in 2.5 oz bottles, which are then packed into a printed carton. Distributed by McNeil-PPC Inc.

    FDA Recall
    Terminated ·Mc-NEIL-PPC, Inc.·Product code NUC·January 25, 2013

    KY TINGLING JELLY Personal Lubricant. The product is packaged into 5 oz tubes with the UPC printed on it. Distributed By: McNeil-PPC Inc.

    FDA Recall
    Terminated ·Mc-NEIL-PPC, Inc.·Product code NUC·January 25, 2013

    Gender PFJ FEMORAL COMP, prosthesis, knee, patello/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/polymer various sizes " Osteoarthritis, traumatic arthritis, polyarthritis, and/or severe chondrocalcinosis of the patellofemoral joint. The salvage of previously failed surgical attempts (e.g., arthroscopy, lateral release, cartilage transplantation). History of patellar dislocation or patella fracture. Dysplasia-induced degeneration. This device is intended for cemented use only."

    FDA Recall
    Terminated ·Zimmer Biomet, Inc.·Product code KRR·January 11, 2016