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

Class 2 Device Recall FIRST RESPONSE

  • 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 FIRST RESPONSE see related information
Date Initiated by Firm October 04, 2023
Date Posted November 07, 2023
Recall Status1 Open3, Classified
Recall Number Z-0266-2024
Recall Event ID 93216
510(K)Number K123436  
Product Classification Kit, test, pregnancy, hcg, over the counter - Product Code LCX
Product FIRST RESPONSE 2 CT, SKU 902343

Code Information All units sold at stores between June 1, 2023 and October 4, 2023.
Recalling Firm/
Family Dollar Stores, Llc.
500 Volvo Pkwy
Chesapeake VA 23320-1604
For Additional Information Contact Customer Service
Manufacturer Reason
for Recall
Products were stored outside of labeled temperature requirements.
FDA Determined
Cause 2
Action On October 4, 2023, Family Dollar notified affected stores. Stores were instructed to check stock and quarantine and discontinue the sale of any affected product. Family Dollar's recall notice was posted online: https://www.familydollar.com/file/general/Posting%20for%20website%2010.6.23%20(2)[3].pdf Affected product was sold at these stores between June 1, 2023 and October 4, 2023. Customers who purchased affected product may return the product to the Family Dollar store where they were purchased without receipt. Customers with questions regarding this recall may contact Family Dollar Customer Service at 844-636-7687 between 9 a.m. and 5 p.m. EST. Customers should contact their physician or health care provider if they have experienced any problems that may be related to using these products.
Quantity in Commerce 329,044 total units
Distribution Distributed to Family Dollar stores in the following states: GA, AL, MS, FL, LA, AR, AZ, KS, TX, OK, CO, NM, NE, UT, NV, WY, ID, SD, ND, CA, MT, OR, WA.
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 = LCX and Original Applicant = CHURCH & DWIGHT CO., INC.