Recall of Device Recall JacksonPratt Hemaduct

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Cardinal Health.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    29739
  • Event Risk Class
    Class 2
  • Event Number
    Z-1406-04
  • Event Initiated Date
    2004-07-28
  • Event Date Posted
    2004-08-25
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2005-02-10
  • Event Source
    USFDA
  • Event Source URL
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    Apparatus, Suction, Single Patient Use, Portable, Nonpowered - Product Code GCY
  • Reason
    The products labeled as sterile are not sterile.
  • Action
    The accounts were telephoned on 7/28/04 and sent follow-up letters on the same date. They were informed that affected lots of products were not sterile, and were requested to inspect their inventory and segregate the product for return to Cardinal Health. The accounts were instructed to call 800-635-6021 for product return and instructions on how to obtain credit and replacement product.

Device

  • Model / Serial
    catalog #JP-HUR880, lot 1040909
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Florida, Arizona, New Jersey and Canada
  • Product Description
    Jackson-Pratt Hemaduct, 15 Fr round, full duct silicone wound drain; a sterile, single use only, Rx device, individually packaged, 10 drains per box, 8 boxes per case; catalog #JP-HUR880; Allegiance Healthcare Corporation, McGaw Park, IL 60085 USA
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Cardinal Health, 1430 Waukegan Rd, McGaw Park IL 60085
  • Source
    USFDA