Drug Recalls Center

1,894 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.

1,894
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
HIGH
FDA DEVICE

GET TESTED INTERNATIONAL AB NAD Profile Test Recall 36 Units for Premarket Approval Issue (2025)

GET TESTED INTERNATIONAL AB recalled 36 NAD Profile Tests distributed nationwide in the United States after regulators found distribution without premarket approval. The devices were distributed without FDA premarket approval or clearance. Patients and healthcare providers should stop using the device immediately and follow recall instructions; contact GET TESTED INTERNATIONAL AB or your health‑ca

GET TESTED INTERNATIONAL AB
Distribution without
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Health & Personal Care
HIGH
FDA DEVICE

GET TESTED INTERNATIONAL AB Vitamin D2 and D3 Test Recall 10 Units Sold Nationwide (2025)

GET TESTED INTERNATIONAL AB recalled 10 Vitamin D2 and D3 Test kits distributed nationwide in the United States. The recall cites distribution without premarket approval or clearance. Patients and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.

GET TESTED INTERNATIONAL AB
Distribution without
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed 780G Insulin Pump Recalled Over Software Issue

Medtronic MiniMed recalled 577 units of the MiniMed 780G insulin pump on November 2, 2025. A software flaw in version 6.60 may cause insulin delivery to suspend unexpectedly, posing serious health risks. Patients should stop using the device immediately and follow recall instructions.

Medtronic MiniMed
A software
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Health & Personal Care
HIGH
FDA DEVICE

Philips IntelliVue Patient Monitor MX800 Recalled for Alarm Failure

Philips North America recalled 1,913,441 IntelliVue Patient Monitors on October 31, 2025. The monitors may fail to alarm, posing a serious risk to patient safety. Healthcare providers and patients should stop using the device immediately and follow recall instructions.

Philips North America
Potential issue
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Health & Personal Care
HIGH
FDA DRUG

Dynashield Skin Protectant Recalled for cGMP Violations

Dyrnarex Corporation recalled 1,560 containers of Dynashield Skin Protectant on October 31, 2025. The product may not meet current Good Manufacturing Practice standards. Consumers should stop using the product immediately and seek guidance from healthcare providers.

DYNASHIELD
cGMP deviations
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Health & Personal Care
HIGH
FDA DRUG

Trifecta Pharmaceuticals Recalls Zinc Oxide Ointment Due to cGMP Deviations

Trifecta Pharmaceuticals recalled 33,000 containers of Globe Zinc Oxide Ointment on October 31, 2025, due to cGMP deviations. Consumers should stop using the product immediately to avoid potential risks. Healthcare providers are advised to contact the company for further guidance.

ZINC OXIDE 20%
cGMP deviations
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Health & Personal Care
HIGH
FDA DRUG

Dynarex Recalls Wecare Calasoothe Ointment Over cGMP Violations

Dynarex Corporation recalled 2,400 containers of Wecare Calasoothe on October 31, 2025, due to cGMP deviations. The recall affects the 4 oz ointment, as it may not meet safety standards. Consumers should stop using the product immediately and consult their healthcare providers.

MENTHOL AND ZINC OXIDE
cGMP deviations
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Health & Personal Care
HIGH
FDA DRUG

Nivagen Zinc Oxide Ointment Recalled Over cGMP Deviations

Nivagen Pharmaceuticals recalled 7,920 bottles of Zinc Oxide Ointment on October 31, 2025. The recall follows cGMP deviations that could impact product safety. Consumers should cease use immediately and consult healthcare providers for advice.

NIVAGEN ZINC OXIDE
cGMP deviations
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Health & Personal Care
HIGH
FDA DRUG

Trifecta Pharmaceuticals Recalls Clotrimazole Cream for cGMP Violations

Trifecta Pharmaceuticals USA recalled 12,150 bottles of Globe Clotrimazole Cream on October 31, 2025. The recall stems from deviations in current Good Manufacturing Practices (cGMP). Consumers should stop using the cream immediately and contact their healthcare providers.

CLOTRIMAZOLE
cGMP deviations
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Health & Personal Care
HIGH
FDA DRUG

Blossom Pharmaceuticals Recalls Lanashield Skin Barrier Over cGMP Violations

Blossom Pharmaceuticals recalled 9,600 containers of Lanashield Skin Barrier on October 31, 2025 due to cGMP deviations. Consumers and healthcare providers should stop using the product immediately. The recall affects products distributed nationwide in the USA.

Blossom Pharmaceuticals
cGMP deviations
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Health & Personal Care
HIGH
FDA DRUG

Dynarex Recalls Moisturizing Wound Hydrogel Over cGMP Violations

Dynarex Corporation recalled 8,184 bottles of Dynagel Moisturizing Wound Hydrogel on October 31, 2025. The recall follows deviations from current Good Manufacturing Practices (cGMP). Consumers should stop using the product immediately and consult healthcare providers for guidance.

Blossom Pharmaceuticals
cGMP deviations
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Health & Personal Care
HIGH
FDA DRUG

Dynarex Recalls Zinc Oxide Ointment Over cGMP Deviations

Dynarex Corporation recalled 2,592 bottles of WeCare Zinc Oxide Ointment on October 31, 2025, due to cGMP deviations. The recall affects products distributed nationwide in the USA. Consumers and healthcare providers must stop using the ointment immediately and seek guidance.

ZINC OXIDE
cGMP deviations
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Health & Personal Care
HIGH
FDA DEVICE

Philips Recalls IntelliVue Patient Monitor Due to Alarm Failure

Philips North America recalled 1,913,441 IntelliVue Patient Monitors on October 31, 2025. The monitors may fail to alarm, posing serious risks to patients. Users must stop using the device immediately and follow the manufacturer's instructions.

Philips North America
Potential issue
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips IntelliVue MP40 Recall 1.9M Monitors Over Alarm Failure (2025)

Philips North America LLC recalled 1,913,441 IntelliVue MP40 patient monitors worldwide after reports the monitors did not alarm. The issue could prevent alerts to clinicians about patient deterioration. Stop using the device and follow the recall instructions from Philips or your healthcare provider immediately.

Philips
Potential issue
Read more
Health & Personal Care
HIGH
FDA DRUG

Dynashield Cream Recalled Due to cGMP Deviations

Dynashield, a 4 oz cream, is recalled after cGMP deviations were identified. The recall affects 7,944 units distributed nationwide. Consumers should stop using the product immediately and contact their healthcare provider for guidance.

DYNASHIELD
cGMP deviations
Read more
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
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Health & Personal Care
HIGH
FDA DRUG

Nivagen Zinc Oxide Ointment Recall 912 Containers Over cGMP Deviations (2025)

Nivagen Zinc Oxide Ointment 20% skin protectant, manufactured in India for Nivagen Pharmaceuticals and distributed nationwide in the USA, is recalled. The recall covers 912 containers. The defect cited is cGMP deviations. Consumers and healthcare providers should stop using the product and follow guidance from Blossom Pharmaceuticals or a healthcare professional.

Nivagen Zinc Oxide
cGMP deviations
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Health & Personal Care
HIGH
FDA DEVICE

Philips IntelliVue MP50 Recall 2025 Over Alarm Failure in 1.9 Million Monitors

Philips North America recalled 1,913,441 IntelliVue MP50 patient monitors worldwide after reports the devices did not alarm. The monitors may fail to alert clinicians to patient deterioration. Hospitals should stop using the devices immediately and follow the manufacturer’s recall instructions.

Philips
Potential issue
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound System Recalled Over Compatibility Issues

Philips Ultrasound recalled 4,819 diagnostic ultrasound systems on October 31, 2025. The recall affects models 795005, 795161, and 989605449841 due to compatibility issues with Apple devices running iOS 18. These issues may prevent the systems from performing live imaging, posing risks in medical settings.

Philips Ultrasound
Ultrasound system
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Health & Personal Care
HIGH
FDA DEVICE

Aizu Olympus OER-Elite Medical Device Recall Affects 6,578 US Units (2025)

Aizu Olympus recalled 6,578 OER-Elite medical devices distributed nationwide in the United States. The recall cites warnings, cautions, and maintenance requirements and says only trained personnel should perform repairs. Healthcare providers and patients should stop using the device and await recall instructions from the manufacturer.

Aizu Olympus
Inform existing
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