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U.S. Department of Health and Human Services

Class 2 Device Recall Urine Reagent Strips (URS) 10 Parameters

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  Class 2 Device Recall Urine Reagent Strips (URS) 10 Parameters see related information
Date Initiated by Firm October 14, 2011
Date Posted January 11, 2012
Recall Status1 Terminated 3 on April 09, 2013
Recall Number Z-0512-2012
Recall Event ID 60476
Product Classification Automated urinalysis system - Product Code KQO
Product Urine Reagent Strips (URS) 11 Parameters

510(K) number: K970250
Devise Listing number: D072377

Each Device consists of 100 strips of Urine Reagent Strips 11 parameters packed with a desiccant pouch inside a black bottle with Cortez Diagnostics Label on the bottle and the bottle placed inside a Cortez Diagnostics Box.
Code Information Product # 2: URS-II-I00G-00I i. Lot Number: 35224 ii. Expiration Date: 08/2013
Recalling Firm/
Teco Diagnostics
1268 N Lakeview Ave
Anaheim CA 92807-1831
For Additional Information Contact Ms. Jenifer Ohta
Manufacturer Reason
for Recall
This recall was initiated in response to findings during a FDA inspection of the firm. The firm's recall has been initiated due to improper manufacture of sub-component nitrite paper Lot 35134, Expiration Date: 01/2014. Discrepancies were found on the information recorded on formulation sheet and manufacturing log sheets. Sampling size submitted for QC testing was insufficient based upon number o
FDA Determined
Cause 2
Nonconforming Material/Component
Action Teco Diagnostics sent an "URGENT: MEDICAL DEVICE RECALL" letter dated October 14, 2011 to affected customers. The letter described the product, problem, and actions to be taken by the customers. The letter instructed customers to examine their inventory for the affected product and to quarantine any product found. A Recall Return Response Form was included with the letter for customers to complete and return. Contact the firm's Technical Support Department at (800) 222-9880 for questions regarding this recall.
Distribution Distributed in CA and Poland.
Total Product Life Cycle TPLC Device Report

1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.