895 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
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 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 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.
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.
Philips North America recalled 28 units of the Cardiac Workstation 5000 on September 12, 2025. A pinched power module wire within the device can cause a short, posing a high risk of electrical hazards. Healthcare providers and patients should stop using the device immediately.
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 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.
Noah Medical recalled 47 units of its Galaxy System on September 12, 2025. Users could not access crucial instructions due to password protection on the user manual. This recall affects distribution in 15 U.S. states and two countries.
UIH Technologies recalled two units of the uEXPLORER MD system on September 12, 2025. Third-party covers can trap between the patient table and gantry, causing mechanical interference. Healthcare providers must stop using the device immediately and follow recall instructions.
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.
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
Argon Medical Devices recalled 1,821 Vena Cava Filter Systems on September 12, 2025. Increased resistance when advancing the dilator poses a risk of injury. The recall affects devices distributed nationwide and internationally.
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.
Major Pharmaceuticals announced a recall of 1,256 blister packs of Chlorpromazine Hydrochloride Tablets on September 12, 2025. The recall stems from the presence of N-Nitroso Desmethyl Chlorpromazine above safe intake levels. Consumers must stop using the product immediately and contact their healthcare provider for guidance.
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.
Major Pharmaceuticals recalled 866 blister packs of Chlorpromazine Hydrochloride Tablets on September 12, 2025. The recall follows the detection of N-Nitroso Desmethyl Chlorpromazine above safe limits. The affected products were distributed nationwide and are classified as a Class II hazard.
Major Pharmaceuticals recalled 506 blister packs of Chlorpromazine Hydrochloride tablets on September 12, 2025. The recall stems from CGMP deviations due to the presence of N-Nitroso Desmethyl Chlorpromazine above safe limits. Consumers should stop using the product immediately and consult healthcare providers.
Major Pharmaceuticals recalled 1,394 blister packs of Chlorpromazine Hydrochloride Tablets due to contamination concerns. The recall occurred on September 12, 2025, after the FDA found N-Nitroso Desmethyl Chlorpromazine above acceptable limits. Consumers should stop using these tablets and seek guidance from healthcare providers.
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.
UIH Technologies recalled 3 units of its uMI 780 MD system on September 12, 2025. The device can trap third-party covers, causing table movement interference. Healthcare providers must stop using the device immediately and follow recall instructions.
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.
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 HealthCare recalled 292 nuclear medicine gamma cameras on September 12, 2025. The devices may have been relocated without proper support, risking detector falls. This poses a serious risk of life-threatening injuries.
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.
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