Health & Personal Care
LOW
FDA DEVICE
GET TESTED INTERNATIONAL AB Female Fertility Test Recalled for Premarket Approval Violation (31Units
Distribution without premarket approval/clearance.
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Distribution without
Recall database
All Product Recalls
Browse 4,434 active product recalls and safety alerts. Use search and filters to narrow the list by product, brand, hazard level, or status.
- Active recalls
- 4,434
- Current page
- 155
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB GI Microbiome Profile Small Recalled for Lack of Premarket Approval (202
Distribution without premarket approval/clearance.
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Distribution without
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB Recalls 184 Menopause FSH Test Kits for Premarket Approval Issue (2025)
Distribution without premarket approval/clearance.
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Distribution without
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB IgE Food Allergy Panel Test Recalled in 2025
Distribution without premarket approval/clearance.
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Distribution without
Health & Personal Care
HIGH
FDA DEVICE
Get Tested International AB 3 in 1 STI Test Recalled for Premarket Approval Issue (2025)
Distribution without premarket approval/clearance.
Get Tested International AB
Distribution without
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB Lyme Test Recalled for 940 Units in 2025
Distribution without premarket approval/clearance.
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Distribution without
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB Chlamydia Test Recall 2026 — 5 US Units Distributed, PMA Issue
Distribution without premarket approval/clearance.
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Distribution without
Health & Personal Care
HIGH
FDA DEVICE
Fresenius Kabi USA Recalls 483 LVP Infusion Sets for IVENIX System Over Incorrect Assembly (2025)
Incorrect assembly of specific lot of LVP Primary Administration Set that could result in serious patient injury.
Fresenius Kabi USA
Incorrect assembly
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB Recalls 3 Food Sensitivity Test Small Units in 2025
Distribution without premarket approval/clearance.
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Distribution without
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL Gut Microbiome Test Large Recalled for Premarket-Approval Violation (2025)
Distribution without premarket approval/clearance.
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Distribution without
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB Parasite Test Recalled for Distribution Without Premarket Approval
Distribution without premarket approval/clearance.
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Distribution without
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB Thyroid TSH Test Recalled Over PMA Issue (1,916 Units)
Distribution without premarket approval/clearance.
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Distribution without
Vehicles & Parts
HIGH
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB DHEA Test Recalled for Premarket-Approval Lapse, 17 Units (2025)
Distribution without premarket approval/clearance.
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Distribution without
Food & Beverages
HIGH
FDA FOOD
Haagen-Dazs Mini Chocolate Bars Recalled for Undeclared Wheat in 2025 (3,410 Cases)
Haagen-Dazs
Undeclared wheat.
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB Candida Test Recalled for 166 Units in 2025
Distribution without premarket approval/clearance.
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Distribution without
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB Allergy Test Small Recalled for Lack of Premarket Approval (2025)
Distribution without premarket approval/clearance.
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Distribution without
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB Recalls Food Intolerance Test Due to Approval Issues
Distribution without premarket approval/clearance.
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Distribution without
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB Recalls Organic Acids Test
GET TESTED INTERNATIONAL AB recalled one unit of its Organic Acids Profile Test Large on November 3, 2025. The recall occurred due to distribution without necessary premarket approval. Patients and healthcare providers should stop using the device immediately.
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Distribution without
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB Medical Device Recalled for Illegal Marketing
Distribution without premarket approval/clearance.
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Distribution without