2,679 recalls tagged with “immediate action”.
FUJIFILM Healthcare Americas Corp recalled 16 CH-200 X-ray machines in the domestic market. The shaft that mounts the X-ray tube unit on the support may break. Protective parts may fail when the shaft breaks during frontward lifting. Healthcare providers should stop using the device immediately and follow recall instructions.
Graviti Pharmaceuticals Private Limited manufactured Bupropion Hydrochloride Extended-Release Tablets XL 300 mg, distributed nationwide by Rising Pharma Holdings, Inc., in 46,512 bottles. The recall cites failed tablet specifications. Stop using the product immediately and contact the manufacturer or your healthcare provider for guidance.
Alcon recalls 28,323 CONSTELLATION Ultravit 10K and CONSTELLATION HyperVit 20K devices used in hospitals worldwide. The recall lists an unspecified hazard. Hospitals should stop using the devices immediately and follow the manufacturer’s instructions. Access the FDA recall notice for details.
Private Label Skin Care recalls Artisan of Skin Benzoyl Peroxide 10% cream after benzene detected. The product was distributed in California and Georgia. Consumers should stop use immediately and contact the company for guidance.
Private Label Skin Care Inc. recalled edunn clarity BP Treatment Cleanser 10% after benzene was detected. The recall covers lot numbers 58170A and 58172A with expiration September 2025. The product was distributed in California and Georgia.
Skin MD by Dr Monika Kiripolsky recalled its Body Acne Cleanser after detecting elevated benzene levels. The recall covers products associated with Lot # 58170A and Lot # 58172A distributed in CA and GA. Consumers should stop use and seek guidance from a healthcare provider.
Private Label Skin Care recalled Micronized BPO Gel Cleanser 10% sold under University Skin Institute in California and Georgia after benzene was detected. The recall is active as of 2025. Consumers should stop using the product immediately and contact the company for guidance.
A benzoyl peroxide acne treatment sold under mel rx Skin by Private Label Skin Care Inc. is recalled for benzene contamination. The recall covers Lot #58170A and 58172A with expiration date 09/2025 and distribution limited to California and Georgia. Consumers should stop using the product immediately and contact the company for guidance.
Torrey Pines Dermatology & Laser Center's Benzaderm BPO Cleanser recall remains active. The FDA-listed recall covers benzoyl peroxide cleanser lot numbers 58170A and 58172A with expiration 09/2025. Consumers should stop use and contact the recall coordinator.
GE HealthCare recalled 1,386 Millennium MG/MC dual-head gamma cameras used in cardiac imaging worldwide. The recall notes devices past End of Guaranteed Service may have been transported without adequate detector support, risking mounting failure and possible detector falls. Facilities should stop using the devices and await recall instructions sent by GE Medical Systems Israel, Functional Imaging
GE HealthCare recalls 64 Elscint Model 4XX dual-head gamma cameras used for cardiac imaging worldwide after discovering potential detector mounting failure during transport. A detector fall could cause life-threatening injuries. Hospitals should stop using the device and follow the manufacturer’s recall instructions.
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.
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
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.
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,
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.
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.
Major Pharmaceuticals recalled 2,064 blister packs of Chlorpromazine Hydrochloride Tablets, 25 mg, sold nationwide through healthcare providers. The recall follows CGMP deviations that allowed the presence of N-Nitroso Desmethyl Chlorpromazine above the allowed limit. Stop using the product immediately and await guidance from Major Pharmaceuticals or your healthcare provider.
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 1,394 blister packs of Chlorpromazine Hydrochloride Tablets, 200 mg, distributed nationwide. The recall cites CGMP deviations with the presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit. Healthcare providers and patients are urged to stop using the product and await guidance from Major Pharmaceuticals and Rugby Laboratories.