1,817 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
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UIH Technologies recalled 11 units of the uCT 760 MD Computed Tomography X-ray System. Third-party outer covers can become trapped between the patient table and gantry, causing mechanical interference during table movement. Hospitals and patients should stop using the device immediately and await manufacturer instructions.
UIH Technologies recalled 2 uEXPLORER MD PET/CT systems after finding third-party outer covers can trap between the patient table and gantry. The interference can occur during table movement. Hospitals and healthcare facilities should stop using the devices and await instructions from UIH Technologies LLC.
UIH Technologies LLC is recalling 4 Shanghai United Imaging Healthcare uMI Panorama 35 MD PET/CT systems sold in the United States. A third-party outer cover can become trapped between the patient table and gantry during table movement. Hospitals and clinics should stop using the devices and follow the manufacturer’s recall instructions.
GE HealthCare recalled 102 dual-head gamma cameras used for cardiac imaging worldwide after finding that some systems past the End of Guaranteed Service could be moved without adequate detector support. This could place excessive stress on detector mounting mechanisms and may cause a detector to fall, posing life-threatening risk. Hospitals and healthcare providers should stop using the devices IM
GE HealthCare Israel recalled 37 Maxicam dual-head gamma cameras distributed worldwide to hospitals. The recall cites potential detector mounting stress if the devices are moved without adequate support. This could result in a detector fall and life-threatening injury. Hospitals and healthcare providers should stop using the device and follow recall instructions from GE HealthCare.
UIH Technologies LLC recalled 95 uMI 550 MD PET/CT systems sold in the United States after reports that third-party outer covers can become trapped between the patient table and gantry. The covers can interfere with table movement during imaging. Hospitals and clinics should stop using the devices and follow the manufacturer's recall instructions immediately.
UIH Technologies LLC recalls eight Shanghai United Imaging uCT 530 MD CT scanners sold to U.S. hospitals. Third‑party outer covers can become trapped between the patient table and gantry, causing mechanical interference during table movement. Hospitals should stop using the device immediately and follow recall instructions from UIH Technologies or their healthcare provider.
Shanghai United Imaging Healthcare recalled 22 CT X-ray systems, including the uCT 550 MD, sold to healthcare facilities in the United States. A third-party outer cover can become trapped between the patient table and gantry, causing mechanical interference during table movement. Stop using the device and follow the manufacturer’s recall instructions immediately.
UIH Technologies LLC recalled 2 units of the uCT ATLAS MD CT X-ray System sold to U.S. health care providers after reports of potential mechanical interference during table movement. The issue involves third-party outer covers that can become trapped between the patient table and gantry. Hospitals should stop using the devices immediately and follow recall instructions from UIH Technologies LLC.
Major Pharmaceuticals recalled 866 Chlorpromazine Hydrochloride 100 mg tablets distributed nationwide after CGMP deviations allowed N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit. The impurity detected raises safety concerns for ongoing use. Stop using the product immediately and contact Harvard Drug Group LLC dba Major Pharmaceuticals or Rugby Laboratories for guidance and,
GE Medical Systems Israel recalls 15 Elscint Varicam dual-head gamma cameras worldwide. The recall cites a risk that devices moved without proper detector support, which could cause a detector fall. Clinicians should stop using the devices and follow manufacturer instructions immediately.
GE HealthCare Israel, Functional Imaging recalled 3 Elscint Helix dual-head gamma cameras worldwide. If moved without adequate detector support, mounting stress could cause a detector fall and life-threatening injury. Hospitals should stop using the device immediately and contact GE Medical Systems Israel, Functional Imaging for instructions.
Major Pharmaceuticals, via The Harvard Drug Group LLC, recalled 506 blister packs of Chlorpromazine Hydrochloride tablets, 50 mg, distributed nationwide. A CGMP deviation shows the presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit. Stop using the product and contact the Harvard Drug Group or Rugby Laboratories for guidance.
Diagnostica Stago recalled 12,740 STA Liatest D-Di units distributed worldwide after a potential risk of underestimating D-Dimer levels. The two listed lots may produce falsely low results. Stop using the devices immediately and follow recall instructions from Diagnostica Stago or your healthcare provider.
Major Pharmaceuticals recalled 1,256 blister packs of Chlorpromazine Hydrochloride tablets, 25 mg, sold nationwide in the United States. A CGMP deviation led to the presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake. Healthcare providers and patients should stop using the product and contact Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories for next-步
GE HealthCare recalled 82 Millenium Myosight dual-head gamma cameras distributed worldwide. The devices could have been moved without adequate detector mounting support. This could cause a detector fall and life-threatening injury. Hospitals and healthcare providers should stop using the cameras immediately and follow manufacturer recall instructions.
GE HealthCare recalled 205 SMV DSXi dual-head nuclear medicine gamma cameras used for cardiac imaging distributed worldwide. The recall cites potential detector mounting stress after End of Guaranteed Service. Hospitals should stop using these devices and follow the manufacturer’s recall instructions. Contact GE Medical Systems Israel Functional Imaging or a healthcare provider for guidance.
Noah Medical recalled 47 Galaxy System bronchoscopic visualization devices distributed to 20 US states and internationally to Hong Kong and Australia. The recall centers on password-protected Instructions for Use. Healthcare providers and patients should stop using the device immediately and follow manufacturer recall instructions.
Argon Medical Devices recalled 1,821 Option Elite Vena Cava Filter System devices sold to U.S. hospitals and international distributors. The recall cites a dilator resistance issue within the introducer sheath that could slow procedures and injure venous tissue. Healthcare providers and patients should stop using the device immediately and follow the recall instructions.
Blueroot Health recalled Bariatric Fusion iron multivitamin bottles after discovering the packaging is not child-resistant. The recall involves two bottle types with 45 mg of iron. Affected bottles lack the required push-down-and-turn caps and carry specific lot numbers. Consumers should stop using the product and contact Blueroot Health for a free child-resistant replacement cap.
Olympus Corporation of the Americas reports an active recall for the BRONCHOVIDEOSCOPE BF-1TH1100. The recall concerns additional IFU updates for safe use with laser, argon plasma coagulation, and high-frequency therapy equipment. The company urges stopping use and following recall instructions.
Olympus Corporation of the Americas recalls 3,250 EVIS EXERA II BF-P180 Bronchovideoscopes sold in the United States and internationally. The recall updates the instructions for use to clarify safe and effective use with laser, argon plasma coagulation, and high-frequency therapy equipment. Healthcare providers should stop using the device immediately and contact Olympus for instructions.
CareFusion 303 BD Alaris infusion pump modules and compatible infusion sets are recalled nationwide in the U.S. and multiple international markets. The recall covers reference numbers including C24101E and 10015414 and related SmartSite components. The defect may cause flow rate and bolus accuracy deviations, and incorrect occlusion timing. Stop using the device and follow recall instructions from
Olympus recalled 262 units of the BF-XT160 bronchoscope after concerns regarding its safe use with laser and high-frequency therapy equipment. Additional instructions for use (IFU) updates clarify potential hazards. Healthcare providers and patients must cease use immediately and follow the manufacturer's recall instructions.
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