Recall of Device Recall HACH SteriChek Sensitive Total Chlorine Reagent Strips, Product 821972

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

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
    48613
  • Event Risk Class
    Class 2
  • Event Number
    Z-2353-2008
  • Event Initiated Date
    2008-05-23
  • Event Date Posted
    2008-09-21
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2012-03-20
  • 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
    Reagent strips - Product Code FKP
  • Reason
    Inconsistencies in total chlorine and free chlorine levels may result in providing inaccurate false positive or false negative results.
  • Action
    The firm initiated phone calls on 5/22/08 and explained the reason for recall and requested the product be quarantined. The customer was informed they would receive a recall letter providing instructions for return, replacement, or credit. During the phone call, some of the customers asked if they should recall to the end user level and they were told to do so, but this instruction was not verbally given to everyone. The recalling firm issued a letter dated 5/23/08 via overnight mail which explained the reason for recall and requested return of the product. The letter requests the customer to notify the end users. A Return Form was enclosed to report the amount of product being returned. The firm telephoned all nonresponders on 7/1-2/08 to assure they received the recall notification. On 7/21/08, the firm issued two different letters flagged as "Expanded Recall Notification" dated 7/21/08. One of the letters covered Product/Part numbers 811909, 812144, and 821972, which were all HACH brands. The other letter covered Product/Part number 812004, which was a private brand. Reason for recall expansion was explained and return of product was requested. If the product was further distributed, subrecall was requested to the end user level. A "Return Form" was enclosed to be completed to indicate the amount of product being returned. Some customers who tried to order product #811909 received a letter dated 7/28/08 informing them they could use their Total Chlorine DPD Test Kit, product #811902, as an alternative method for testing. For assistance, contact Hach Customer Service at 1-800-548-4381, ext. 3563.

Device

  • Model / Serial
    Lot numbers 6233, 6278, 6313, 6326, 6341, 7039, 7071, 7092, 7127, 7171, 7193, 7213, 7253, 7255, 7302, 7339, 7339, 8008, 8029, 8063, 8081, 8096, 8125, and 8150
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide and Foreign distribution to Canada and Denmark.
  • Product Description
    HACH SteriChek Sensitive Total Chlorine Reagent Strips, Tests for water and rinse water down to 0.1 mg/l (ppm), packaged 1/100-strip btl. per carton, 12 cartons per shipping case, Product #821972. The firm name on the label is HACH Company, Ames, IA. The product is used in measuring for low levels of total chlorine (including chloramines and free chlorine) in feed water used to prepare dialysate.
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Hach Co, 100 Dayton Ave, Ames IA 50010-6402
  • Manufacturer Parent Company (2017)
  • Source
    USFDA