Recall of Device Recall CaviCide

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

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
    62864
  • Event Risk Class
    Class 2
  • Event Number
    Z-2267-2012
  • Event Initiated Date
    2012-02-06
  • Event Date Posted
    2012-08-24
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2012-08-24
  • 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
    Disinfectant, medical devices - Product Code LRJ
  • Reason
    Metrex research is recalling cavicide containing the spring fresh fragrance because the affected lot of product containing this fragance has caused an increase in reported health reactions in some individuals such as headache, nausea, and respiratory discomfort.
  • Action
    Metrex sent an "URGENT: MEDICAL DEVICE RECALL" letter dated February 16, 2012 to all affected customers. The letter identifies the product, problem, and actions to be taken by the customers. A Mandatory Recall Response Form was attached for customers to complete and return via fax to 734-947-6725. Contact Customer Care Center at (800) 841-1428 for questions regarding this recall.

Device

  • Model / Serial
    CaviCide Lot # 10-1301, 10-2301, 10-2302, 10-2328, 10-2328A, 10-2328B, 10-2331, 10-2333, 10-1334, 10-2334, 10-1335, 10-2335, 10-1342A, 10-1343, 10-2345.  EnviroCide Lot # 10-2331.  Backscratchers Cavicide lot # 10-1342.  MaxiSpray Plus lot # 10-2328A and 10-1343.  pdCARE Surface Disinfectant lot # 10-2331 and 10-2345.  Z3 Surface Disinfectant lot # 10-2328.
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution-USA (nationwide) and the countries of Canada, AE, and YE.
  • Product Description
    CaviCide, Part Numbers: 13-1025, 13-1000, 13-1024, MC-1000. || Alternate brands: || EnviroCide, part number: 13-3325. || Private labeled products of Cavicide: || Backscratchers Cavicide, part number: 13-4800. || MaxiSpray Plus, part numbers: 13-7400 and 13-7405. || pdCARE Surface Disinfectant, part numbers: 13-7525 and 13-7500. || Z3 Surface Disinfectant, part number: 13-7900. || CaviCide is a multi-purpose disinfectant/decontaminant cleaner for use on hard, non-porous inanimate surfaces. CaviCide is a bactericidal, virucidal, fungicidal, and tuberulocidal which is available in a ready-to-use, liquid form typically contained in 1 gallon bottles, 2.5 gallon bottles, 25 oz. spray bottles, or 55 gallon drums (depending on the item number). CaviCide may also be branded as a private label (see (1)(vi) below for names and Table 1 above for additional details). The product may be used (1) for precleaning non-instrument surfaces prior to disinfection; (2) for precleaning instruments prior to disinfection; (3) as a virucide on non-instrument surfaces; (4) as a disinfectant on non-instrument surfaces; (5) as a virucide on precleaned non-critical medical devices, instruments and implements; and (6) as a disinfectant on precleaned non-critical medical devices, instruments, and instruments. It is useful in health care settings such as hospitals, emergency medical settings, surgical centers, isolation areas, neonatal units, patient care areas, ophthalmic and optometric facilities, dental offices, dental operatories, animal care facilities, salon settings, emergency vehicles, schools, health club facilities, kitchens, bathrooms, prisons, morgues, and other critical care areas.
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Metrex Research, LLC., 28210 Wick Rd, Romulus MI 48174-2639
  • Manufacturer Parent Company (2017)
  • Source
    USFDA