Devices

Device Recall Extremity Pack

  • Modèle / numéro de série
    Lot number and expiration date  84476, 7/21/2018
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed in AZ, CA, CO, CT, FL, GA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NV, OH, PA, TX, UT, VA, and WA.
  • Description du dispositif
    Extremity Pack-N Brunswick, part number PSS1866(A
  • Manufacturer
    Windstone Medical Packaging, Inc.
  • 1 Event

Fabricant

Windstone Medical Packaging, Inc.
  • Adresse du fabricant
    Windstone Medical Packaging, Inc., 1602 4th Ave N, Billings MT 59101-1521
  • Société-mère du fabricant (2017)
    Windstone Medical Packaging Inc.
  • Source
    USFDA

3 dispositifs médicaux avec un nom similaire

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Device Recall EXTREMITY PACK
  • Modèle / numéro de série
    Code:9002615 Lots: 140915322 exp. 10/31/15 141015728 exp. 11/30/15 141015728 exp. 11/30/15 141216308 exp. 12/31/15 150116556 exp. 1/1/16 150518786 exp. 5/31/16
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Distributed Only in Puerto Rico.
  • Description du dispositif
    EXTREMITY PACK 4/CS || Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. || .
  • Manufacturer
    Customed, Inc
Device Recall Extremity Pack
  • Modèle / numéro de série
    Lot number and expiration date  100226, 9/11/2019 101400, 10/7/2019 84373, 5/28/2018 84678, 6/8/2018 84896, 5/26/2018 84959, 7/29/2018 85470, 2/23/2017 85505, 7/23/2018 85547, 8/23/2018 85695, 7/8/2018 85846, 8/5/2018 86258, 9/19/2018 86509, 9/28/2018 86663, 8/11/2019 86686, 9/9/2018 86908, 9/13/2018 87155, 9/16/2018 87730, 7/5/2017 87968, 9/6/2018 88008, 7/1/2017 88862, 2/7/2018 89394, 11/15/2017 89546, 7/21/2017 89832, 12/29/2018 95313, 9/16/2019 95453, 1/22/2019 95880, 6/12/2019 96000, 1/6/2019 96383, 5/25/2018 96384, 5/13/2018 96923, 5/1/2019 97709, 5/1/2019 99376, 6/7/2019
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed in AZ, CA, CO, CT, FL, GA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NV, OH, PA, TX, UT, VA, and WA.
  • Description du dispositif
    Extremity Pack, part number AMS3240 || Extremity Pack, part number AMS4764 || Extremity Pack, part number AMS4788(A || Extremity Pack, part number PSS1798(A || Extremity Pack, part number PSS1798(A || Extremity Pack, part number PSS1798(A || Extremity Pack, part number PSS1842(A || Extremity Pack, part number PSS1842(A || Extremity Pack, part number PSS1842(A || Extremity Pack, part number PSS1842(A || Extremity Pack, part number PSS2706 || Extremity Pack, part number PSS2706 || Extremity Pack, part number PSS2706 || Extremity Pack, part numbre PSS2706 || Extremity Pack, part number PSS2706 || Extremity Pack, part number PSS2706 || Extremity Pack, part number PSS2706 || Extremity Pack, part number PSS2706 || Extremity Pack, part number PSS2706 || Extremity Pack, part number PSS2706 || Extremity Pack, part number PSS2706(A || Extremity Pack, part number PSS2706(A || Extremity Pack, part number PSS2706(A || Extremity Pack, part number PSS2706(A
  • Manufacturer
    Windstone Medical Packaging, Inc.
Device Recall Extremity Pack
  • Modèle / numéro de série
    Lot number and expiration date  101250, 10/8/2019
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed in AZ, CA, CO, CT, FL, GA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NV, OH, PA, TX, UT, VA, and WA.
  • Description du dispositif
    Extremity Pack (1344), part number AMS6561
  • Manufacturer
    Windstone Medical Packaging, Inc.