895 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
GET TESTED INTERNATIONAL AB recalled one unit of its Drug Test Small on November 3, 2025. The recall occurred due to distribution without premarket approval or clearance. The FDA classified this recall as Class II, indicating a high risk to patients and healthcare providers.
GET TESTED INTERNATIONAL AB recalled six units of its Food Intolerance Test on November 3, 2025. The recall stems from the distribution of the product without premarket approval or clearance. Healthcare providers and patients must stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 528 syphilis test units on November 3, 2025. The recall follows the distribution of the test without necessary premarket approval. Patients and healthcare providers should stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 45 units of its Intestinal Worms Test on November 3, 2025. The recall stems from distribution without necessary premarket approval or clearance. Healthcare providers and patients must stop using the product immediately.
GET TESTED INTERNATIONAL AB recalled 50 units of its Heavy Metals Test on November 3, 2025. The recall follows distribution without premarket approval or clearance, posing potential health risks. Healthcare providers and patients must stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 17 units of its Adrenal Test on November 3, 2025. The recall occurred due to distribution without premarket approval or clearance. Patients and healthcare providers must stop using the device immediately.
Orthofix U.S. recalled 19,431 units of its FIREBIRD SI Fusion System on November 3, 2025. The recall stems from inconsistent labeling claims that may mislead users. Affected models include multiple sizes of FIREBIRD SI Screws, sold worldwide.
Orthofix U.S. LLC recalled 13,317 PTC Spacer Systems on November 3, 2025, due to inconsistent labeling claims. The recall affects multiple model numbers sold worldwide, including in the U.S. The company advises immediate cessation of use and communication with healthcare providers.
GET TESTED INTERNATIONAL AB recalled 109 units of its Candida Test on November 3, 2025. The recall stems from distribution without premarket approval or clearance. Patients and healthcare providers should stop using this device immediately.
GET TESTED INTERNATIONAL AB recalled 76 units of its Allergy Test on November 3, 2025. The recall occurred due to distribution without premarket approval. Patients and healthcare providers should stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 258 HPV Antigen Tests on November 3, 2025. The tests were distributed nationwide without premarket approval or clearance. Healthcare providers and patients must stop using these devices immediately.
GET TESTED INTERNATIONAL AB recalled one unit of its Alcohol Test Saliva on November 3, 2025, due to distribution without premarket approval. The recall affects the entire lot of this medical device. Consumers and healthcare providers must stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 29 Pet Allergy Test units on November 3, 2025. The recall follows distribution without premarket approval. Patients and healthcare providers must stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 2,043 units of its 8 in 1 STI Test Kit on November 3, 2025. The recall resulted from distribution without premarket approval. Patients and healthcare providers must stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 19 units of its Allergy Test on November 3, 2025. The recall stems from distribution without premarket approval or clearance. Patients and healthcare providers must stop using the device immediately.
GET TESTED INTERNATIONAL AB recalled 115 units of its Iron Deficiency 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 80 cholesterol test devices on November 3, 2025. The recall occurred due to distribution without premarket approval. Patients should stop using the devices immediately and follow the manufacturer’s instructions.
GET TESTED INTERNATIONAL AB recalled 19 units of its Hair Mineral Analysis device on November 3, 2025. The recall follows distribution without premarket approval or clearance. This action affects devices distributed nationwide in the U.S.
GET TESTED INTERNATIONAL AB recalled four units of its Organic Acids Test on November 3, 2025. The recall stems from distribution without premarket approval or clearance. Healthcare providers and patients must stop using the device immediately and follow the manufacturer's instructions.
GET TESTED INTERNATIONAL AB recalled three units of its Biological Age & Longevity Test on November 3, 2025, due to distribution without necessary premarket approval. The recall affects products distributed nationwide in the U.S.
GET TESTED INTERNATIONAL AB recalled 47 blood type tests on November 3, 2025. The recall results from distribution without premarket approval. Patients and healthcare providers must stop using the device immediately and follow manufacturer instructions.
GET TESTED INTERNATIONAL AB recalled 754 units of its 2 in 1 Trichomonas / Gardnerella Test on November 3, 2025. The recall follows distribution without premarket approval. Patients and healthcare providers must stop using the product immediately.
GET TESTED INTERNATIONAL AB recalled 31 units of the Leaky Gut Test 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 10 units of its Vitamin D2 and D3 Test on November 3, 2025. The recall follows distribution without premarket approval. Patients and healthcare providers must stop using the device immediately.
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