Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB Heavy Metals Test Recall for 50 Units (2025)
Distribution without premarket approval/clearance.
GET TESTED INTERNATIONAL AB
Distribution without
Drug Recalls Center
2,090 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
2,090
Total Drug Recalls
24
High Risk Medications
FDA
Official Source
Important Medication Safety Information
- Do not stop taking prescribed medications without consulting your healthcare provider
- Contact your pharmacist or doctor if you have a recalled medication
- Check lot numbers carefully - not all batches may be affected
- Return recalled medications to your pharmacy for proper disposal
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
Health & Personal Care
LOW
FDA DEVICE
GET TESTED INTERNATIONAL AB Intestinal Worms Test Recalled for 45 Units Nationwide in 2025
Distribution without premarket approval/clearance.
GET TESTED INTERNATIONAL AB
Distribution without
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB Recalled 6 Food Intolerance Test Large Units for Premarket Issue (2025)
Distribution without premarket approval/clearance.
GET TESTED INTERNATIONAL AB
Distribution without
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB Food Sensitivity Test Large Recalled for 3 Units in 2025
Distribution without premarket approval/clearance.
GET TESTED INTERNATIONAL AB
Distribution without
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB Recalls 6 Gut Microbiome Test Small Kits for Premarket Approval Violate
Distribution without premarket approval/clearance.
GET TESTED INTERNATIONAL AB
Distribution without
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB Medical Device Recalled for Illegal Marketing
Distribution without premarket approval/clearance.
GET TESTED INTERNATIONAL AB
Distribution without
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB SIBO Test Recall: 55 Units in US Over Premarket Approval (2025)
GET TESTED INTERNATIONAL AB's SIBO Test was distributed nationwide in the United States. The device was distributed without FDA premarket approval or clearance. Stop using the device immediately and follow the recall instructions from the manufacturer.
GET TESTED INTERNATIONAL AB
Distribution without
Health & Personal Care
HIGH
FDA DEVICE
GET TESTED INTERNATIONAL AB Trichomonas Vaginalis Test Recalled for Lack of Premarket Approval (2025
Distribution without premarket approval/clearance.
GET TESTED INTERNATIONAL AB
Distribution without
Health & Personal Care
HIGH
FDA DEVICE
Medtronic MiniMed 780G Insulin Pump Recalled Over Software Issue
A software timing and processor communication issue in MiniMed" 780G software version 6.60 may trigger Pump Error 43 and/or Pump Error 41, resulting in suspension of insulin delivery.
Medtronic MiniMed
A software
Health & Personal Care
HIGH
FDA DEVICE
Philips IntelliVue MP2 Monitors Recalled for Alarm Failure in 2025 (1,913,441 Units)
Philips North America is recalling 1,913,441 IntelliVue MP2 patient monitors worldwide. The devices may fail to alarm when critical conditions arise. Hospitals should stop using the monitors and follow Philips recall instructions.
Philips
Potential issue
Health & Personal Care
HIGH
FDA DRUG
Nivagen Zinc Oxide Ointment Recall 912 Containers Over cGMP Deviations (2025)
Nivagen Zinc Oxide
cGMP deviations
Health & Personal Care
HIGH
FDA DEVICE
Philips IntelliVue MP30 Monitors Recalled for Alarm Failure
Philips North America recalled 1,913,441 IntelliVue MP30 monitors on October 31, 2025. The devices may fail to alarm, posing a serious risk to patients. Users must stop using the monitors and follow recall instructions immediately.
Philips North America
Potential issue
Health & Personal Care
HIGH
FDA DEVICE
Aizu Olympus OER-Elite Medical Device Recall Affects 6,578 US Units (2025)
Aizu Olympus
Inform existing
Health & Personal Care
HIGH
FDA DRUG
Trifecta Pharmaceuticals Recalls Zinc Oxide Ointment Due to cGMP Deviations
ZINC OXIDE 20%
cGMP deviations
Health & Personal Care
HIGH
FDA DEVICE
Philips IntelliVue MP20 Recall Expands to 1.9 Million Units Over Alarm Failure Risk (2025)
Philips recalls 1.913 million IntelliVue MP20 patient monitors worldwide because the devices may fail to alarm. The issue could prevent critical alerts from sounding. Hospitals should stop using the monitors immediately and follow Philips recall instructions.
Philips
Potential issue
Health & Personal Care
HIGH
FDA DEVICE
Philips IntelliVue MP60 Recall for Alarm Failure Affects 1,913,441 Monitors (2025)
Philips North America is recalling 1,913,441 IntelliVue MP60 patient monitors. The monitors may fail to alarm as designed. Hospitals and clinics using MP60 units should stop using the devices and follow the recall instructions.
Philips
Potential issue
Health & Personal Care
HIGH
FDA DEVICE
Stryker MV3 Bariatric Bed Recalled Over Compatibility Issues
Stryker Medical recalled 286 MV3 bariatric beds on October 31, 2025. The beds may not be compatible with Arise 1000EX mattresses, posing risks to patients. Healthcare providers and patients must stop using the beds immediately.
Stryker Medical Division of Stryker
Stryker has
Health & Personal Care
HIGH
FDA DEVICE
Philips IntelliVue MP40 Recall 1.9M Monitors Over Alarm Failure (2025)
Potential issue where the IntelliVue monitors did not alarm.
Philips
Potential issue
Health & Personal Care
HIGH
FDA DRUG
Trifecta Pharmaceuticals Recalls Clotrimazole Cream Over cGMP Issues
CLOTRIMAZOLE
cGMP deviations
Health & Personal Care
HIGH
FDA DEVICE
Philips IntelliVue MP5 M8105A Recall: 1,913,441 Monitors Worldwide Alarm Failure (2025)
Potential issue where the IntelliVue monitors did not alarm.
Philips
Potential issue
Health & Personal Care
HIGH
FDA DEVICE
Philips IntelliVue Patient Monitor MX800 Recalled for Alarm Failure
Potential issue where the IntelliVue monitors did not alarm.
Philips North America
Potential issue
Health & Personal Care
HIGH
FDA DRUG
Nivagen Zinc Oxide Ointment Recalled Due to cGMP Deviations
NIVAGEN ZINC OXIDE
cGMP deviations
Health & Personal Care
HIGH
FDA DEVICE
Philips IntelliVue MP90 Monitors Recalled Over Alarm Failure
Philips North America recalled 1,913,441 IntelliVue MP90 monitors on October 31, 2025. The monitors may fail to alarm, posing a high risk to patient safety. Users must stop using the devices immediately and follow manufacturer instructions for remedy.
Philips North America
Potential issue
Health & Personal Care
HIGH
FDA DEVICE
Philips Ultrasound System Recalled Over Compatibility Issues
Ultrasound system compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imagining.
Philips Ultrasound
Ultrasound system
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