Data Foundry

Medical device recalls 2023

VERIQUICK PREGNANCY TEST 1CT — Class II medical device recall Z-0264-2024

Ongoing recall by Family Dollar Stores, Llc., reported 2023-11-15, distributed in AL, AR, AZ, CA, CO, FL, GA, ID…. Products were stored outside of labeled temperature requirements.

Recall numberZ-0264-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmFamily Dollar Stores, Llc., Chesapeake, VA, United States
Recall initiated2023-10-04
Classified2023-11-07
Reported by FDA2023-11-15
DistributedAL, AR, AZ, CA, CO, FL, GA, ID, KS, LA, MS, MT, ND, NE, NM, NV, OK, OR, SD, TX, UT, WA, WY
Quantity329,044 units
Reason classeslabeling

Product

VERIQUICK PREGNANCY TEST 1CT, SKU 901260

Reason for recall

Products were stored outside of labeled temperature requirements.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0264-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.