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U.S. Department of Health and Human Services

Class 2 Device Recall Walgreens At Home A1C Test Kit

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  Class 2 Device Recall Walgreens At Home A1C Test Kit see related information
Date Initiated by Firm December 02, 2016
Create Date December 13, 2019
Recall Status1 Terminated 3 on July 16, 2020
Recall Number Z-0684-2020
Recall Event ID 84231
510(K)Number K090413  
Product Classification Assay, glycosylated hemoglobin - Product Code LCP
Product Walgreens At-Home A1C Test Kit, Software Version Revision D, REF Number 3056
Code Information Lot Numbers: 1606405 1610622 1610910
Recalling Firm/
Manufacturer		 Polymer Technology Systems
4600 Anson Blvd
Whitestown IN 46075
Manufacturer Reason
for Recall		 A numerical value less than 4% or greater than 13% may be displayed instead of the expected <4% or >13% result, due to a software bug.
FDA Determined
Cause 2		 Software design
Action A Customer Bulletin dated November 2016 was distributed to customers.
Quantity in Commerce 15,118
Distribution The products were distributed to the following US states: AR, CA, FL, IL, IN, KY, MN, NC, NJ, NY, OH, PA, RI TN, UT, VA, WA, and Puerto Rico. The products were distributed to the following foreign countries: Australia, Bahamas, Belgium, Bahrain, Bangladesh, Canada, China, Columbia, Czech Republic, England, Egypt, Greece, Spain, India, Indonesia, Haiti, Hong Kong, Italy, Japan, Jordan, Kenya, Lebanon, Mexico, Myanmar, Malaysia, Philippines, Pakistan, South Africa, Nigeria, Poland, Saudi Arabia, Sweden, Turkey, Singapore, Trinidad & Tobago, Slovenia, Vietnam, United Arab Emirates, Uruguay.
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.
510(K) Database 510(K)s with Product Code = LCP and Original Applicant = BAYER HEALTHCARE, LLC
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