Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Class 2 Device Recall Walgreens Quick Read Digital Thermometer

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
  Class 2 Device Recall Walgreens Quick Read Digital Thermometer see related information
Date Initiated by Firm November 23, 2011
Date Posted January 11, 2012
Recall Status1 Terminated 3 on August 14, 2017
Recall Number Z-0506-2012
Recall Event ID 60581
510(K)Number K041516  
Product Classification digital thermometer - Product Code FLL
Product Walgreens Quick Read Digital Thermometer; an electronic digital thermometer; Model WIC551226
Code Information Model WIC551226, UPC 31191708790, all lots.
Recalling Firm/
Manufacturer		 Walgreen Company
200 Wilmot Rd # 3395
Deerfield IL 60015-4620
For Additional Information Contact Walgreens Product Quality Dept.
847-315-2755
Manufacturer Reason
for Recall		 The thermometers have been reported to have inaccurate readings
FDA Determined
Cause 2		 Labeling design
Action On November 23, 2011, Walgreens issued a recall notice electronically to their stores, instructing them to pull and quarantine the Thermometers and placing a Stop Scan on the products in the computer cash register system on the same date. Walgreens also removed the thermometer from their internet sales site.
Quantity in Commerce estimated 92,000 units
Distribution Nationwide through Walgreens retail stores and their internet site.
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 = FLL and Original Applicant = VEGA TECHNOLOGIES, INC.
-
-