BEUDAMED
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    Filters FDA Recall × Status: Terminated × Clear all

    Vitrectomy Pack, part number AMS4952 Product packaged in a convenient manner for use in a general clinical procedure

    FDA Recall
    Terminated ·Windstone Medical Packaging, Inc.·Product code FSY·March 16, 2017

    ENT Pack, part number AMS2727 Product packaged in a convenient manner for use in a general clinical procedure

    FDA Recall
    Terminated ·Windstone Medical Packaging, Inc.·Product code FSY·March 16, 2017

    PRK Tray, part number DDS1044 Product packaged in a convenient manner for use in a general clinical procedure

    FDA Recall
    Terminated ·Windstone Medical Packaging, Inc.·Product code FSY·March 16, 2017

    Vitrectomy Kit, part number CMP1016(A. Product packaged in a convenient manner for use in a general clinical procedure

    FDA Recall
    Terminated ·Windstone Medical Packaging, Inc.·Product code FSY·March 16, 2017

    Minor Operation Kit, part number AMS1530 Product packaged in a convenient manner for use in a general clinical procedure

    FDA Recall
    Terminated ·Windstone Medical Packaging, Inc.·Product code FSY·March 16, 2017

    Lasik Tray, part number DDS1045-2 Product packaged in a convenient manner for use in a general clinical procedure

    FDA Recall
    Terminated ·Windstone Medical Packaging, Inc.·Product code FSY·March 16, 2017

    Ortho Basic Pack, part number AMS6459 Product packaged in a convenient manner for use in a general clinical procedure

    FDA Recall
    Terminated ·Windstone Medical Packaging, Inc.·Product code FSY·March 16, 2017

    Setup Pack, part number AMS3112(A Product packaged in a convenient manner for use in a general clinical procedure

    FDA Recall
    Terminated ·Windstone Medical Packaging, Inc.·Product code FSY·March 16, 2017

    Ophthalmic Pack, Part number WAL1107(A and WAL1190 Product packaged in a convenient manner for use in a general clinical procedure

    FDA Recall
    Terminated ·Windstone Medical Packaging, Inc.·Product code FSY·March 16, 2017

    Cataract Kit - Dr. Slingsby, part number CMP1017(B. Product packaged in a convenient manner for use in a general clinical procedure

    FDA Recall
    Terminated ·Windstone Medical Packaging, Inc.·Product code FSY·March 16, 2017

    Cataract Kit, part numbers CAT1467AM and CAT1538(B. Product packaged in a convenient manner for use in a general clinical procedure

    FDA Recall
    Terminated ·Windstone Medical Packaging, Inc.·Product code FSY·March 16, 2017

    Custom Tray, part numbers PSS1111 and PSS1111(A. Product packaged in a convenient manner for use in a general clinical procedure

    FDA Recall
    Terminated ·Windstone Medical Packaging, Inc.·Product code FSY·March 16, 2017

    Dicken Eye Pack, part number CPA-3202-2. Product packaged in a convenient manner for use in a general clinical procedure

    FDA Recall
    Terminated ·Windstone Medical Packaging, Inc.·Product code FSY·March 16, 2017

    Eye Pack, part numbers WAL1085(B and WAL1085(C\ Product packaged in a convenient manner for use in a general clinical procedure

    FDA Recall
    Terminated ·Windstone Medical Packaging, Inc.·Product code FSY·March 16, 2017

    Eye Cataract Pack, part numbers AMS1359 and AMS1359-1 Product packaged in a convenient manner for use in a general clinical procedure

    FDA Recall
    Terminated ·Windstone Medical Packaging, Inc.·Product code FSY·March 16, 2017

    Dr. Wischmeier Pack, part numbers: AMS3509 and AMS3509(A Product packaged in a convenient manner for use in a general clinical procedure

    FDA Recall
    Terminated ·Windstone Medical Packaging, Inc.·Product code FSY·March 16, 2017

    Plastic Pack, part numbers AMS1028, AMS1028(A, and WAL1189. Product packaged in a convenient manner for use in a general clinical procedure

    FDA Recall
    Terminated ·Windstone Medical Packaging, Inc.·Product code FSY·March 16, 2017

    iLink Bone Void Filler. Packaged in a double Tyvek pouch, then placed in a box. Model Number: 50-05-0010, Exp. 2010-04.

    FDA Recall
    Terminated ·Theken Spine LLC·Product code MQV·August 26, 2008

    Scimed ChoICE PT ''J'' Tip 182 cm Guide Wire, a single use, sterile (EO), device packaged in a carrier tube, which is held in a coil by plastic clips. The carrier tube assembly of the guide wire is sealed into a pouch. The pouch assembies are packaged in a five-pack product box.

    FDA Recall
    Terminated ·Symbiosis Corp.·Product code DQX·July 16, 2002

    AxIEM Touch N Go Pointer Probe. Model Number: 9735318. Placed in a 30mil PETG tray sealed with a Tyvek lid and then placed in a shelf carton.

    FDA Recall
    Terminated ·Medtronic Navigation, Inc.·Product code HAW·December 12, 2016