These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
2,251 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
GET TESTED INTERNATIONAL AB recalled 100 units of its Kidney Test on November 3, 2025. The recall addresses distribution without necessary premarket approval. Patients and healthcare providers should stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 36 units of the NAD Profile Test on November 3, 2025. The recall was issued due to distribution without premarket approval. Patients and healthcare providers should stop using this device immediately.
GET TESTED INTERNATIONAL AB recalled two units of its Gut Microbiome Test on November 3, 2025. The recall stems from distribution without necessary premarket approval or clearance. Patients and healthcare providers should stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 12 units of the Serotonin Test on November 3, 2025. The recall occurred due to distribution without premarket approval. Patients and healthcare providers must stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 17 units of its DHEA Test on November 3, 2025. The recall resulted from distribution without premarket approval or clearance. Patients and healthcare providers must stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled one sperm test on November 3, 2025. The recall stems from distribution without premarket approval. Patients and healthcare providers should stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 658 units of its Parasite Test on November 3, 2025. The recall is due to distribution without premarket approval or clearance. Patients and healthcare providers should stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 463 gonorrhea tests on November 3, 2025. The recall follows distribution without premarket approval or clearance. Patients and healthcare providers must stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled four MPOX Test units on November 3, 2025. The recall stems from distribution without premarket approval or clearance. Healthcare providers and patients must stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 13 units of its Iodine Test on November 3, 2025. The product was distributed without necessary premarket approval. Healthcare providers and patients must stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 1,361 herpes tests on November 3, 2025. The recall stems from distribution without premarket approval. Patients and healthcare providers must stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 148 units of its Diabetes HbA1c Test on November 3, 2025. The recall stems from distribution without premarket approval. Patients and healthcare providers must stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 1,218 D-Dimer Tests on November 3, 2025, due to distribution without premarket approval. The recall affects units distributed nationwide in the U.S. Patients and healthcare providers must stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled eight units of the Fructose Intolerance Test on November 3, 2025. The recall occurs due to distribution without premarket approval. Patients and healthcare providers should stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 12 units of its Peptic Ulcer Test on November 3, 2025, due to distribution without premarket approval. The recall affects devices distributed nationwide in the United States.
GET TESTED INTERNATIONAL AB recalled 1,557 Vitamin D-Tests on November 3, 2025, due to distribution without premarket approval. The recall affects devices distributed nationwide in the United States. Consumers should stop using the test immediately and follow manufacturer instructions.
GET TESTED INTERNATIONAL AB recalled the GI Microbiome Profile XL on November 3, 2025, due to distribution without premarket approval. Three units were distributed nationwide in the U.S. Patients and healthcare providers should stop using this device immediately.
GET TESTED INTERNATIONAL AB recalled 18 units of Neurotransmitters Plus on November 3, 2025. The recall occurred due to distribution without premarket approval or clearance. Patients should cease use immediately and follow manufacturer instructions.
GET TESTED INTERNATIONAL AB recalled 94 units of its Parasite Test on November 3, 2025. The recall stems from distribution without premarket approval or clearance. Patients should stop using the device immediately and follow provided instructions.
GET TESTED INTERNATIONAL AB recalled 10 units of the Pollen Allergy Test on November 3, 2025. The recall stems from distribution without necessary premarket approval. Patients should stop using the device immediately and follow manufacturer instructions.