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 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 DRUG

Nivagen Zinc Oxide Ointment Recalled Due to cGMP Deviations

Nivagen Pharmaceuticals recalled 13,536 containers of zinc oxide ointment on October 31, 2025. The recall follows deviations from current Good Manufacturing Practices (cGMP). Consumers must stop using the product immediately and contact healthcare providers for guidance.

NIVAGEN ZINC OXIDE
cGMP deviations
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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 DEVICE

STRYKER NICO Myriad Handpiece Recall for 39,148 Units Worldwide (2026)

STRYKER recalled 39,148 NICO Myriad Handpieces sold worldwide due to latex in packaging that could trigger allergic reactions. The latex-containing tape secures components within packaging. Healthcare providers and patients should stop using the device immediately and follow the recall instructions from Stryker.

Stryker
Tape used
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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
Read more
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

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 DRUG

Dynarex Recalls Wecare Enema Due to Safety Violations

Dynarex Corporation recalled 18,912 containers of Wecare Enema on October 31, 2025, due to cGMP deviations. Consumers should stop using the product immediately. The recall affects products distributed nationwide in the USA.

SALINE ENEMA
cGMP deviations
Read more
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
Read more
Health & Personal Care
HIGH
FDA DRUG

Trifecta Pharmaceuticals Recalls Clotrimazole Cream Over cGMP Issues

Trifecta Pharmaceuticals recalled 14,700 bottles of Globe Clotrimazole Cream USP on October 31, 2025, due to significant cGMP deviations. The affected product may not meet necessary safety and quality standards. Consumers should stop using the cream immediately and seek guidance from healthcare providers.

CLOTRIMAZOLE
cGMP deviations
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

Olympus HX-400U-30 Recall: 7,803 Endoscopic Ligation Devices Recalled in 2025

Olympus Corporation of the Americas recalled 7,803 HX-400U-30 single‑use ligating devices distributed nationwide in the United States. The ligation loop may fail to release or detach. Hospitals and clinics should stop using the device immediately and follow the recall instructions from Olympus or their healthcare providers.

Olympus
Potential that
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recall Affects 286,400 Units Across Global Pumps (2025)

B. Braun Medical recalls 286,400 IV administration sets used with Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump worldwide. The devices may backflow from secondary IV containers into primary containers and cannot be primed. Stop using the device immediately and follow recall instructions from the manufacturer.

B. Braun Medical
Potential for
Read more
Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Set Recall 2025 Affects 6,768 Units Over Backflow Risk

6,768 IV administration sets are recalled worldwide by B Braun Medical. The recall covers devices used with gravity and pump systems. The hazard is potential backflow of medication into primary IV containers and inability to prime. Stop using the product and follow the recall instructions immediately. Contact B Braun Medical for instructions via the FDA recall page linked below.

B Braun Medical
Potential for
Read more
Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recalled for 126,050 Units Over Backflow Risk (2025)

B. Braun Medical recalled 126,050 IV administration sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The recall cites potential backflow from secondary to primary IV containers and an inability to prime. Health care providers and patients should stop using the device immediately and follow recall instructions from the manufacturer.

B. Braun Medical
Potential for
Read more
Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Recalls 15,250 PB1500 IV Set Over Backflow Risk (2025)

B. Braun Medical recalled 15,250 PB1500 15-DROP IV SETS distributed worldwide, including the US, Canada, Germany, Guatemala and Singapore. The devices pose a backflow risk from secondary IV containers into primary containers and may fail to prime. Healthcare facilities should stop using the product and follow recall instructions.

B. Braun Medical
Potential for
Read more
Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recall for 187,464 Units Over Backflow Risk (2025)

B. Braun Medical recalled 187,464 IV administration sets worldwide, including US distribution and shipments to Canada, Germany, Guatemala, and Singapore. The devices pose a backflow risk from secondary (piggyback) IV containers into primary containers and can fail to prime properly. Healthcare providers and patients should stop using the devices immediately and follow recall instructions.

B. Braun Medical
Potential for
Read more
Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Set Recall Affects 2,544 Units Worldwide

B Braun Medical Inc recalled 2,544 IV administration sets due to risk of backflow from secondary piggyback containers into primary IV lines and inability to prime. The recall covers products used with BBMI Infusomat Space, Outlook, and Vista Basic pumps and distributed worldwide including the US, Canada, Germany, Guatemala and Singapore. Patients should stop using the device immediately and follow

B Braun Medical
Potential for
Read more
Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Sets Recalled for Backflow Risk and Occlusion (2025)

B Braun Medical Inc. recalls 111,312 IV Administration Sets worldwide, including US and international markets, due to backflow risk and occlusion. The recall affects catalog numbers 490193 and 490326, used with Infusomat Space, Outlook, and Vista Basic pumps. Stop using immediately and follow recall instructions for refunds or replacements.

B Braun Medical
Potential for
Read more
Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Recalls 32,500 Caresite Extension Sets for IV Pumps (2025)

B. Braun Medical recalled 32,500 Caresite Extension Sets used with Infusomat Space, Outlook, and Vista Basic IV pumps worldwide. The devices pose a backflow and occlusion risk in the primary IV line. Hospitals and healthcare providers should stop using the device immediately and follow the recall instructions.

B. Braun Medical
Potential for
Read more
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