Every recall we track for Universal Meditech Inc. — 28 in all — plus the complaints and injury reports the public filed about them.
Universal Meditech recalls unapproved pregnancy test strips due to lack of FDA marketing authorization and inability to verify safety documentation. Affected products were manufactured after March 2021.
Universal Meditech recalls Am I Pregnant? One Step HCG Pregnancy Test REF 100-17 due to unverified safety and lack of post-market support. Products may not meet FDA standards without proper documentation.
Universal Meditech recalls PrestiBio breastmilk alcohol test strips (model 910-10) due to lack of FDA verification and potential safety risks. All units made after March 2021 are affected.
Universal Meditech recalls To Life hCG Pregnancy Urine Test Strips due to unverified safety and regulatory compliance. The recall follows the company's closure and inability to provide documentation for product safety.
Universal Meditech Inc. recalls HealthyWiser KetoFast Ketone Test Strips REF 900-1K due to unverified manufacturing compliance and lack of post-market documentation. Consumers should check product details and contact the company for updates.
Universal Meditech recalls One Step Ovulation Test REF 200-01 due to unverified safety and regulatory compliance issues. The company is going out of business and cannot fulfill post-market responsibilities.
Universal Meditech recalls Lem Fertility LH Ovulation Test strips (REF 200-07) due to unverified safety and lack of post-market documentation. Products made after March 2021 may be unsafe without proper regulatory compliance.
Universal Meditech recalls DiagnosUS Ovulation Predictor Midstream REF 200-17 due to unverified safety and lack of post-market documentation. Products manufactured after March 2021 are affected.
Universal Meditech recalls HealthyWiser pH test strips due to unverified safety and regulatory compliance issues. The company is going out of business and cannot fulfill post-market responsibilities.
Universal Meditech recalls DiagnosUS hCG Pregnancy Urine Test Strips (REF 100-12) due to unverified safety and lack of post-market documentation. All units made after March 2021 are affected.
Universal Meditech Inc. recalls HealthyWiser UTI Test Strips (REF 900-UTI) due to lack of FDA approval and unverified quality control. Consumers should stop using these unapproved tests to avoid potential safety risks.
Universal Meditech recalls DiagnosUS hCG Pregnancy Test Cassette Format REF 100-27 due to unverified safety and regulatory compliance. All units made after March 2021 are affected.
Universal Meditech recalls DiagnosUS One Step LH Ovulation Test Strips (REF 200-07) due to unverified safety and regulatory compliance. Products made after March 2021 may pose risks without proper documentation.
Universal Meditech recalls DiagnosUS hCG Pregnancy Urine Test Cassette Format REF 100-13 due to unverified safety and regulatory compliance. All units made after March 2021 are affected.
Universal Meditech recalls PrestiBio Ovulation and Pregnancy Strips (REF 100-4, 200-4) sold after March 2021 due to lack of FDA verification and potential safety risks. Consumers should contact the company for details.
Universal Meditech recalls DiagnosUS One Step FSH Menopausal Test strips (REF 210-07) due to unverified manufacturing compliance and lack of post-market documentation. All units made after March 2021 are affected.
Universal Meditech recalls PrestiBio Ovulation Strips (REF 200-4) due to unverified safety and lack of post-market support. All units made after March 2021 are affected.
Universal Meditech recalls HealthyWiser UriTest 10-Parameter Reagent Test Strips (REF 900-10) due to unverified safety and lack of post-market support as the company goes out of business.
Universal Meditech recalls One Step Pregnancy Test REF 100-01 due to unverified safety and regulatory compliance issues. The company is going out of business and cannot fulfill post-market responsibilities.
Universal Meditech recalls Ovulation Test Strips REF 200-07 due to unverified safety and lack of post-market support. Products made after March 2021 may pose risks without proper documentation.
Universal Meditech recalls DeTec hCG Pregnancy Urine Test Cassettes due to unverified safety and regulatory compliance issues. Products may not meet FDA standards without proper documentation.
Universal Meditech recalls Lem Fertility hCG Pregnancy Urine Test REF 100-12 due to unverified quality and safety documentation. Products made after March 2021 may have unknown performance risks.
Universal Meditech recalls PrestiBio Ketone Test Strips (model 900-1KET) due to unverified safety and lack of post-market support. All units made after March 2021 are affected.
Universal Meditech recalls DiagnosUS Pregnancy Test Midstream REF 100-17 due to unverified quality and safety documentation. Products made after March 2021 may have unknown performance characteristics.
Universal Meditech recalls unapproved PrestiBio test strips due to lack of FDA marketing authorization and inability to verify safety documentation. Products made after March 2021 are affected.
Universal Meditech recalls PrestiBio Rapid Detection Pregnancy Test Midstream REF 100-17 3 TESTS due to unverified safety and lack of post-market support. All units made after March 2021 are affected.
Universal Meditech recalls DiagnosUS SARS-CoV-2 Antibody tests due to unverified manufacturing and lack of post-market documentation. Products made after March 2021 may have unknown safety and effectiveness.
Universal Meditech Inc. recalls Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kits sold without FDA approval. Products labeled as green and white boxes with model numbers 550-10. Consumers should check labels for lot numbers.
