• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Class 3 Device Recall PTS Panels CHOLGLU Test Strips

  • 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 3 Device Recall PTS Panels CHOLGLU Test Strips see related information
Date Initiated by Firm August 16, 2022
Create Date September 14, 2022
Recall Status1 Open3, Classified
Recall Number Z-1741-2022
Recall Event ID 90791
510(K)Number K162282  
Product Classification Glucose oxidase, glucose - Product Code CGA
Product PTS Panels CHOL+GLU Test Strips (REF 1765)
Code Information Complete UDI: (01)00381931765016(17)230627(10)A202 UPC Code: 381931765016 lot A202
Recalling Firm/
Polymer Technology Systems, Inc. dba PTS Diagnostics, Inc.
4600 Anson Blvd
Whitestown IN 46075-4489
For Additional Information Contact PTS Diagnostics Customer Service
Manufacturer Reason
for Recall
Incorrect instructions for use were packaged into the final product.
FDA Determined
Cause 2
Labeling Change Control
Action PTS Diagnostics notified customers on August 16, 2022, through an Urgent Medical Device Recall letter. Customers were instructed to return product for replacement. Distributors were asked to forward the notice to all customers/users who may have received the product. If you have any questions, please contact PTS Diagnostics' Customer Service directly, Monday through Friday, 8:00 AM to 5:00 PM, Eastern Time at +1 317-870-5610 or 877-570-8610 (U.S. toll-free).
Distribution Worldwide distribution - US Nationwide distribution in the state of Virginia and the countries of Japan and Russia.
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 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
510(K) Database 510(K)s with Product Code = CGA and Original Applicant = Polymer Technology Systems, Inc. d/b/a PTS Diagnostics