Recall of Brain Heart Infusion Agar (BHIA)

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

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
    39367
  • Event Risk Class
    Class 2
  • Event Number
    Z-0011-2008
  • Event Initiated Date
    2007-08-17
  • Event Date Posted
    2007-10-10
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2011-06-07
  • 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
    Microbiological media plates - Product Code JSO
  • Reason
    Marketed a regulated product without a 510(k).
  • Action
    Firm notified consignees by phone and fax on August 17, 2007, instructing them to destroy the product.

Device

  • Model / Serial
    PML's catalog #P1174, LOT CODES: 75707-1, 75975-1, 76285-1, 235823-1, 236361-1, 236916-1, 237354-1, 237378-1, 237917-1
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    US, Puerto Rico, & Canada
  • Product Description
    Brain Heart Infusion Agar (BHIA) + Vancomycin 6 MCG/ML || Microbiological media plates
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Pml Microbiologicals Inc., 27120 Sw 95th Ave, P.o. Box 570, Wilsonville OR 97070
  • Source
    USFDA