Drug Recalls Center

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

514
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.

HIGHFDA DEVICE

UIH Technologies Recalls X-ray System Over Mechanical Hazard

UIH Technologies recalled 8 units of its uCT 530 MD X-ray system on September 12, 2025. Third-party outer covers can trap between the patient table and gantry, causing mechanical interference. Healthcare providers and patients must stop using the device immediately.

UIH Technologies
Third-party outer
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HIGHFDA DEVICE

Shanghai United Imaging X-ray System Recalled Due to Mechanical Hazard

Shanghai United Imaging Healthcare Co., Ltd. recalled 22 units of its uCT 550 MD X-ray system on September 12, 2025. The recall was issued after reports that third-party outer covers can trap between the patient table and gantry. This can cause mechanical interference during table movement, posing a high risk to patients and healthcare providers.

UIH Technologies
Third-party outer
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HIGHFDA DEVICE

Shanghai United Imaging Recalls CT X-ray System Due to Hazard

Shanghai United Imaging Healthcare Co., Ltd. recalled 11 units of its uCT 760 MD Computed Tomography X-ray System on September 12, 2025. The recall addresses a serious hazard where third-party outer covers can become trapped between the patient table and gantry, leading to mechanical interference. Healthcare providers and patients must stop using the device immediately and follow recall directives

UIH Technologies
Third-party outer
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HIGHFDA DEVICE

GE HealthCare Recalls Nuclear Medicine Gamma Cameras Over Fall Risk

GE HealthCare recalled 1,386 nuclear medicine gamma cameras on September 12, 2025. Certain models may have been relocated without proper support, risking detector integrity. This could lead to life-threatening injuries from falls.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
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HIGHFDA DEVICE

GE HealthCare Recalls Gamma Cameras Due to Fall Hazard

GE HealthCare recalled 102 dual-head nuclear medicine gamma cameras on September 12, 2025. The recall stems from inadequate support during transportation that could lead to a detector fall, posing a life-threatening injury risk. The affected devices are past their End of Guaranteed Service and should not be used immediately.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
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HIGHFDA DEVICE

GE HealthCare Recalls Nuclear Medicine Camera Over Fall Risk

GE HealthCare recalled three units of the Elscint Helix nuclear medicine gamma camera on September 12, 2025. The recall affects systems that may have been transported without proper support, risking detector falls. This issue poses a high risk of life-threatening injuries.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
Read more
HIGHFDA DEVICE

UIH Technologies Recalls PET/CT System Over Mechanical Hazard

Shanghai United Imaging Healthcare Co., Ltd. recalled four units of its Positron Emission Tomography and Computed Tomography System on September 12, 2025. The recall stems from a risk of mechanical interference during table movement due to third-party outer covers. Healthcare providers and patients must stop using the device immediately.

UIH Technologies
Third-party outer
Read more
HIGHFDA DEVICE

GE HealthCare Recalls Nuclear Medicine Gamma Cameras Over Fall Risk

GE HealthCare recalled 54 nuclear medicine gamma cameras on September 12, 2025. The recall affects devices that may have been transported without proper detector support. This issue poses a high risk of detector falls, potentially leading to serious injuries.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
Read more
HIGHFDA DEVICE

GE Healthcare Recalls Nuclear Medicine Cameras Due to Fall Risk

GE HealthCare recalled 15 nuclear medicine gamma cameras on September 12, 2025. The recall affects systems that may have been relocated without proper support, risking detector falls. This poses a significant danger of life-threatening injuries to patients and healthcare providers.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
Read more
HIGHFDA DEVICE

GE HealthCare Recalls Cardial Nuclear Medicine Cameras Over Fall Risk

GE HealthCare recalled 11 Cardial nuclear medicine gamma cameras on September 12, 2025. The recall follows concerns over inadequate detector support potentially leading to life-threatening falls. The affected systems were transported without proper safeguards, compromising safety.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
Read more
HIGHFDA DEVICE

GE HealthCare Recalls Nuclear Medicine Gamma Camera Due to Fall Risk

GE HealthCare recalled 45 dual-head nuclear medicine gamma cameras on September 12, 2025. The recall affects devices that may have been relocated without proper support, risking a detector fall. This defect can lead to life-threatening injuries.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
Read more
HIGHFDA DEVICE

GE HealthCare Recalls Nuclear Medicine Camera Over Fall Risk

GE HealthCare recalled 37 nuclear medicine gamma cameras on September 12, 2025. The recall follows concerns that inadequate detector support during transport could lead to life-threatening falls. The affected systems are past the End of Guaranteed Service and pose serious risks to patients and healthcare providers.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
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HIGHFDA DRUG

Unique Pharmaceuticals Recalls Cetirizine Tablets Over Wrong ID Imprint

Unique Pharmaceuticals Labs recalled 9,936 bottles of Cetirizine Hydrochloride Tablets on September 12, 2025. The tablets were imprinted with the wrong ID, posing a potential health risk. Consumers should stop using the product immediately and seek guidance from healthcare providers.

CETIRIZINE HYDROCHLORIDE
Tablet/Capsules Imprinted
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HIGHFDA DEVICE

UIH Technologies Issues Recall for Computed Tomography X-ray System

Shanghai United Imaging Healthcare recalled two units of the uCT ATLAS MD X-ray system on September 12, 2025. The recall follows reports that third-party outer covers can trap between the patient table and gantry, leading to mechanical interference. Healthcare providers and patients must cease use immediately and follow manufacturer instructions.

UIH Technologies
Third-party outer
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HIGHFDA DEVICE

GE HealthCare Recalls Nuclear Medicine Camera Over Fall Risk

GE HealthCare recalled 28 dual-head gamma cameras on September 12, 2025. The recall comes after concerns that inadequate support during relocation could lead to a detector fall. This situation poses a high risk of life-threatening injury.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
Read more
HIGHFDA DEVICE

Shanghai United Imaging Healthcare Recalls X-ray System Due to Hazard

Shanghai United Imaging Healthcare Co., Ltd. recalled two units of its uCT 780 MD Computed Tomography X-ray System on September 12, 2025. Third-party outer covers can trap between the patient table and gantry, causing mechanical interference. This recall affects units distributed in the US and internationally.

UIH Technologies
Third-party outer
Read more
HIGHFDA DEVICE

UIH Technologies Recalls PET/CT System Due to Mechanical Hazard

UIH Technologies recalled 95 units of its uMI 550 Positron Emission Tomography and Computed Tomography System on September 12, 2025. Third-party outer covers can trap between the patient table and gantry, posing a mechanical interference risk. Patients and healthcare providers must stop using the device immediately.

UIH Technologies
Third-party outer
Read more
HIGHFDA DEVICE

GE HealthCare Recalls Nuclear Medicine Gamma Camera Over Fall Risk

GE HealthCare recalled 64 units of the Elscint Model 4XX gamma camera on September 12, 2025. The recall affects systems that lack adequate support during transport, risking detector falls. If the detectors fall, they can cause serious injuries to patients and healthcare providers.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
Read more
HIGHFDA DEVICE

GE HealthCare Issues Recall of Nuclear Medicine Camera Due to Fall Risk

GE HealthCare recalled a dual-head nuclear medicine gamma camera on September 12, 2025, after identifying a risk of detector falls. One unit is affected, posing a high risk of life-threatening injury. Users must stop using the device immediately and follow manufacturer instructions.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
Read more
HIGHFDA DEVICE

GE HealthCare Recalls Gamma Camera Due to Fall Hazard

GE HealthCare recalled 82 units of the Millenium Myosight gamma camera on September 12, 2025. The recall affects systems that may lack sufficient support during transport, posing a risk of detector falls. This defect can result in life-threatening injuries.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
Read more
HIGHFDA DEVICE

GE Medical Systems Recalls Nuclear Medicine Gamma Cameras Over Hazard

GE HealthCare recalled 205 dual-head nuclear medicine gamma cameras on September 12, 2025. The recall affects models that may have been relocated without proper detector support, leading to potential falls. This issue poses a high risk of life-threatening injury.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
Read more

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