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Open, Classified

VERIQUICK PREGNANCY TEST 1CT, SKU 901260

FDA Recall Z-0264-2024 · Posted 2023-11-07

Recalling FirmFamily Dollar Stores, Llc.
Recall StatusOpen, Classified
Product CodeLCX
Date Initiated2023-10-04
Product Quantity329,044 total units

Reason for Recall

Products were stored outside of labeled temperature requirements.

Firm 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.

Root Cause

Storage

Distribution Pattern

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.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K123703HEALGEN HCG ONE STEP PREGNANCY TEST (STRIP), HEALGEN HCG ONE STEP PREGNANCY TEST (CASSETTE)Healgen Scientific,, LLC · 2013-04-10

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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