Drug Recalls Center

1,817 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.

1,817
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

Olympus BF-XT40 Bronchoscope Recall Affects 821 Units Worldwide in 2025

Olympus Corporation of the Americas issued a Class I recall for 821 BF-XT40 bronchoscopes worldwide, including 116 units in the United States and 705 outside the U.S. The recall centers on updated Instructions For Use to clarify safe and effective use with laser, argon plasma coagulation and high-frequency therapy equipment. Hospitals and clinics should stop using the devices and follow Olympus’召v

Olympus Corporation of the Americas
Additional IFU
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Health & Personal Care
HIGH
FDA DEVICE

Olympus BF-1T60 Bronchofiberscope Recall for IFU Updates (2025)

Olympus recalled 3,216 BF-1T60 bronchofiberscopes distributed nationwide and internationally after updating instructions for safe use with laser, argon plasma coagulation and high-frequency therapy equipment. The recall updates guidance to reduce risk during advanced energy-device procedures. Clinicians and facilities should stop using the devices and follow manufacturer instructions for recall.

Olympus Corporation of the Americas
Additional IFU
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Health & Personal Care
CRITICAL
FDA DEVICE

Abbott TactiFlex Sensor Ablation Catheter Recall 2025 Affects 1,958 Units

Abbott recalled 1,958 TactiFlex Sensor Enabled Ablation Catheters worldwide. A limited number of tip detachment events occurred during catheter removal from packaging. Patients and healthcare providers should stop using the device immediately and follow Abbott's recall instructions.

Abbott
Abbott has
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Health & Personal Care
HIGH
FDA DEVICE

Biomet Juggerknot Mini Soft Anchors 912080 Recall 40 Units Nationwide 2025

Biomet recalled 40 Juggerknot Mini Soft Anchors, model 912080, distributed nationwide in the United States. The outer carton label lists JuggerKnot 1.0mm Mini devices, but the cartons contain JuggerKnot 1.4mm Short devices. Patients and clinicians should stop using the device and follow the recall instructions provided by Biomet.

Biomet
The outer
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Health & Personal Care
HIGH
FDA DEVICE

Draeger Atlan A350XL Anesthesia Workstation Recalled for Ventilator Failure Risk (223 Units) in 25+N

Draeger recalls 223 Atlan A350XL anesthesia workstations distributed in 25 states and many countries after reports of piston ventilator failure and mechanical ventilation failures. The recall affects units imported from Draegerwerk AG and Co. KGaA. Stop using the device immediately. Contact Draeger for instructions and patient safety guidance.

Draeger
The device
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Health & Personal Care
HIGH
FDA DEVICE

BioPro Recalls 147 Metal and Ceramic Femoral Heads Over Sterility Packaging Issue

BioPro recalled 147 femoral head components distributed in the US. The devices cover metal cobalt chromium and ceramic heads in sizes 22, 28, 32, 36 and 40 millimeters. The recall cites a packaging defect that could compromise the sterile barrier. If implanted, the loss of sterility could pose infection risk. Hospitals and surgeons should follow BioPro recall instructions immediately.

BioPro
Potential packaging
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Health & Personal Care
HIGH
FDA DEVICE

NOXBOX Recalled 1,667 NOxBOXi Nitric Oxide Delivery System Units in 2025

NOXBOX recalled 1,667 NOxBOXi Nitric Oxide Delivery System units sold in Tennessee. The recall was issued Sept. 9, 2025. An internal fault can occur when users press the interface rapidly without waiting for the device to respond. Healthcare providers and patients should stop using the device immediately and follow manufacturer recall instructions.

NOXBOX
The unexpected
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Health & Personal Care
HIGH
FDA DEVICE

NOXBOX NOxBOXi Nitric Oxide Delivery System Recalled for 1,667 Units in 2025

NOXBOX LTD recalled 1,667 NOxBOXi Nitric Oxide Delivery System units distributed in Tennessee after reports of flow and dose fluctuations. The device can show fluctuations when the total flow through its sensor drops below 0.5 LPM. Dose fluctuations have been observed with LifePulse HFJV or conventional ventilators under certain settings. Stop using the device immediately and follow the recall. NO

NOXBOX
Fluctuations may
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Health & Personal Care
HIGH
FDA DEVICE

BioPro Femoral Head Hip Implant Recall 147 Units in 2025 Texas and Michigan

BioPro recalled 147 BioPro Femoral Head hip implant components sold in Texas and Michigan after a packaging defect could compromise sterility. The defect may result in loss of sterility, creating a risk of infection if implanted. Hospitals and clinicians should stop using the devices and await manufacturer instructions.

BioPro
Potential packaging
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Health & Personal Care
HIGH
FDA DEVICE

BioPro Endo Head Ceramic Recall Affects 147 Units Over Sterility Packaging Issue (2025)

BioPro recalled 147 Endo Head Ceramic implant components distributed in Texas and Michigan after packaging could compromise the sterile barrier. The defect could result in loss of sterility of the device, creating an infection risk if implanted. Clinicians and patients should stop using the devices and contact BioPro for instructions and refunds.

BioPro
Potential packaging
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Health & Personal Care
HIGH
FDA DEVICE

MedicalCommunications GmbH Recalls 474 Ashvins HEYEX 2 / HEYEX PACS Software Units (2025)

MedicalCommunications GmbH recalled 474 Ashvins HEYEX 2 / HEYEX PACS software units distributed nationwide in the United States. The affected software versions range from 2.6.0 (Build 2088) to 2.6.8 (Build 2220). The hazard is that the measured value may be smaller than the actual area, potentially affecting imaging measurements. Stop using the software immediately and follow manufacturer recall‑s

MedicalCommunications
Potential that
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Health & Personal Care
HIGH
FDA DEVICE

Draeger Atlan A350 Anesthesia Workstations Recalled for Ventilator Failures in 2025

Drӕager recalled 530 Atlan A350 anesthesia workstations imported from Draegerwerk AG and Co. KGaA and distributed to 25 U.S. states and more than 30 countries. The device can experience a piston ventilator failure before use or fail to ventilate during use. Hospitals should stop using affected units immediately and follow Draeger recall instructions.

Draeger
The device
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Health & Personal Care
HIGH
FDA DEVICE

Iantrek C-Rex UNO CRX-120 Goniotomy Instrument Recalled for Packaging Integrity Issue (2025)

Iantrek recalled 198 C-Rex UNO Microinterventional Goniotomy Instruments, CRX-120 models, distributed nationwide to healthcare facilities. The recall cites potential compromised integrity of the sterile packaging. Healthcare providers and patients should stop using the device immediately and follow recall instructions via the manufacturer.

Iantrek
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Spacelabs Healthcare DVI Display Cables Recalled for EMI Risk in 16,898 Units (2025)

Spacelabs Healthcare is recalling 16,898 DVI display cables worldwide, including the United States. The cables are used as external display connectors for certain monitors. The recall follows a risk that inadequately shielded cables may cause electromagnetic interference with other medical devices. Stop using the affected cables immediately and await manufacturer instructions.

Spacelabs Healthcare
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Philips X7-2 Ultrasound Transducer Recall for 5 Units Nationwide (2026)

Philips Ultrasound recalled 5 X7-2 ultrasound transducers distributed nationwide to healthcare providers. The recall is to provide clarification and labeling to define the useful life of ultrasound transducers in the field. Healthcare facilities should stop using the recalled devices and follow Philips Ultrasound, Inc instructions or contact their provider for guidance.

Philips Ultrasound
To provide
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Health & Personal Care
HIGH
FDA DRUG

Endo USA Recalls 1,041 Cartons of Everolimus 5mg Tablets Over IP-C Impurity (2025)

Endo USA, Inc. recalled 1,041 cartons of Everolimus 5mg tablets nationwide in the United States due to an impurity IP-C out of specification. The impurity IP-C is out of specification in the drug product. Patients and healthcare providers should stop using this product immediately and contact Endo USA or their healthcare provider for guidance.

Everolimus
Failed Impurities/Degradation
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Health & Personal Care
HIGH
FDA DEVICE

Philips Recal Size 40 L12-5 Ultrasound Transducers for Labeling Life Span Recall (2026)

Philips recalled 40 L12-5 ultrasound transducers distributed nationwide in the United States after regulators flagged labeling to define the devices' useful life. The recall concerns labeling clarity rather than a device malfunction. Healthcare providers and patients should stop using the device immediately and await instructions from Philips Ultrasound, Inc or their healthcare provider.

Philips Ultrasound
To provide
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Health & Personal Care
LOW
FDA DEVICE

Philips 3D6-2 Ultrasound Transducer Recalled for Labeling Clarification (17 Units, 2025)

Philips recalled 17 units of the 3D6-2 Ultrasound Transducer distributed nationwide to healthcare facilities in the United States. The recall seeks to clarify labeling defining the transducer’s useful life. Clinicians and facilities should stop using the device immediately and follow Philips recall instructions.

Philips Ultrasound
To provide
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