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Early Blush Pregnancy Test (3 HCG Midstreams)

Equinox Biotech Co., Ltd. · Model 82191 · UDI-DI 06938444982191

LCX
10
510(k) clearances
236
Adverse events
25
Recalls
119
Facilities

Description

Early Blush Pregnancy Test (3 HCG Midstreams) is intended for the qualitative determination of human chorionic gonadotropin (hCG) in the urine to aid in early detection of pregnancy. There are 3 6mm midstreams in one box.

Recalls

DateFirmReason
2025-12-26GOLD STAR DISTRIBUTION INCPotential exposure of rodents and rodent activity in the distribution center.
2025-11-03GET TESTED INTERNATIONAL ABDistribution without premarket approval/clearance.
2023-10-04Family Dollar Stores, Llc.Products were stored outside of labeled temperature requirements.
2023-10-04Family Dollar Stores, Llc.Products were stored outside of labeled temperature requirements.
2023-10-04Family Dollar Stores, Llc.Products were stored outside of labeled temperature requirements.
2023-05-22Universal Meditech Inc.Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk Alcohol Test Strip, DiagnosUS SARS-CoV-2 Antibody (IgG/IgM) Test, HealthyWiser KetoFast" Ketone Test Stri
2023-05-22Universal Meditech Inc.Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk Alcohol Test Strip, DiagnosUS SARS-CoV-2 Antibody (IgG/IgM) Test, HealthyWiser KetoFast" Ketone Test Stri
2023-05-22Universal Meditech Inc.Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk Alcohol Test Strip, DiagnosUS SARS-CoV-2 Antibody (IgG/IgM) Test, HealthyWiser KetoFast" Ketone Test Stri
2023-05-22Universal Meditech Inc.Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk Alcohol Test Strip, DiagnosUS SARS-CoV-2 Antibody (IgG/IgM) Test, HealthyWiser KetoFast" Ketone Test Stri
2023-05-22Universal Meditech Inc.Universal Meditech Inc. was violatively distributing PrestiBio" Breastmilk Alcohol Test Strip, DiagnosUS SARS-CoV-2 Antibody (IgG/IgM) Test, HealthyWiser KetoFast" Ketone Test Stri

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.