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    Imalux Niris OCT Imaging System Probe, Model Number 1300, Serial Number F464019, IMALUX Corporation, Cleveland, OH The Niris Imaging System probe is used with the Niris Imaging System. The Niris Imaging System employs Optical Coherence Tomography (OCT), which can be used to construct high spatial resolution. The probe, is attached to the Imaging Console, and is used to direct light to and from the patient tissue. A small electromechanical scanning mechanism in the probe moves the optical beam laterally across the tissue surface while simultaneously acquiring in-depth backscattering profile at each lateral position. The probe is not labeled or sold as sterile.

    FDA Recall
    Terminated ·Imalux Corporation·Product code NQQ·December 22, 2011

    OXIRIS SET, Product Code 112016; Dialyzer, High Permeability With Or Without Sealed Dialysate System

    FDA Recall
    Open, Classified ·VANTIVE US HEALTHCARE LLC·Product code KDI·January 6, 2026

    DuoDERM" Extra Thin dressings are highly flexible, control gel formula dressings designed for use on dry to lightly exudating wounds. DuoDERM" Extra Thin dressings are particularly suitable in areas subject to friction and those requiring contouring, e.g., elbows, heels. DuoDERM" Extra Thin dressings interact with wound moisture producing a soft mass that enables removal of the dressing with little or no damage to newly formed tissues. They help isolate the wound against bacterial and other external contamination. INDICATIONS " Management of superficial, dry to lightly exudating dermal ulcers. " Post-operative wounds. " Protective dressings.

    FDA Recall
    Open, Classified ·ConvaTec, Inc·Product code NAD·August 29, 2025

    Radiesse, Injectable Implant - 1.3cc Syringe, Sterile, Sterilized Using Steam, Use Before 2013-01, Ref 8046M7, Lot 1024417, Manufactured by: BioForm Medical Inc, 4133 Courtney Rd #10 Franksville, WI 53126. Subdermal implantation for the correction of moderate to severe facial wrinkles and folds, such as masolabial folds and it is also intended for restoration and/or correction of the signs of facial fat loss (lipoatrophy) in people with human immunodeficiency virus.

    FDA Recall
    Terminated ·Merz Aesthetics, Inc.·Product code LMH·April 6, 2011

    Medtronic SynchroMed II, Model 8637-40, Programmable pump

    FDA Recall
    Open, Classified ·Medtronic Neuromodulation·Product code LKK·November 13, 2023

    Medtronic SynchroMed II, Model 8637-20, Programmable pump

    FDA Recall
    Open, Classified ·Medtronic Neuromodulation·Product code LKK·November 13, 2023