Devices

Device Recall Orthocord Blue Braided Composite Suture

  • Model / Serial
    Lot # Expiration Date AP2547 2011-11-30 12:00AM
  • Product Classification
    General and Plastic Surgery Devices
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    Worldwide Distribution -- USA, Argentina, Australia, Belgium, Brazil, Canada, Chile, China, Colombia, Denmark, Greece, Hong Kong, Israel, Japan, Korea, Luxemburg, Mexico, New Zealand, Norway, Panama, Puerto Rico, Sweden, Taiwan, United Kingdom, Uruguay, and Venezuela.
  • Product Description
    Orthocord Blue Braided Composite Suture, DePuy Mitek, A Johnson & Johnson Company, Meets USP and EP, except for diameter. || DePuy Mitek, Inc. || 325 Paramount Drive, Raynham, MA 02767 || Sutures are intended for general soft tissue approximation and/or ligation.
  • Manufacturer
    Ethicon, Inc.
  • 1 Event

Manufacturer

Ethicon, Inc.
  • Manufacturer Address
    Ethicon, Inc., US Highway 22 West, Somerville NJ 08876
  • Manufacturer Parent Company (2017)
    Johnson & Johnson
  • Source
    USFDA

One device with a similar name

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Device Recall ORTHOCORD BLUE BRAIDED COMPOSITE SUTURE 2
  • Model / Serial
    ALL from Jan 1 2010 - Corrected IFU implementation date
  • Product Classification
    General and Plastic Surgery Devices
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    Nationwide Distribution.
  • Product Description
    ORTHOCORD BLUE BRAIDED COMPOSITE SUTURE 2 (5 METRIC), Catalog Number: 223111. || For use in general soft tissue approximation, and/or ligation, including orthopedic procedures.
  • Manufacturer
    DePuy Mitek, Inc., a Johnson & Johnson Co.