2,756 recalls tagged with “immediate action”.
Baxter Healthcare Corp. is recalling 18,720 CLEARLINK System Non-DEHP Conti-Flo Soln Sets sold nationwide in the United States. The IV sets may leak, potentially compromising therapy. Patients and healthcare providers should stop using the device immediately and contact Baxter Healthcare for instructions.
Fresenius Medical Care recalls 172,494,732 Optiflux High Flux E-beam Dialyzers distributed nationwide in the United States. Caps on these dialyzers were changed from threaded to press-on versions, requiring users to press the caps firmly to secure them. Patients and healthcare providers should stop using these devices immediately and follow recall instructions issued by the manufacturer.
Northeast Scientific recalled 173 units of the NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter distributed nationwide to U.S. healthcare facilities. The device is not cleared for marketing in the United States due to sterility concerns. A breach in the sterile barrier packaging could compromise sterility. Health care providers and patients should stop using the device immediately.
Northeast Scientific Corp. recalled 1,019 units of the NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter. The model is not cleared for marketing in the United States. The recall cites potential breaches in sterile barrier packaging that could compromise sterility. Patients and healthcare providers should stop using the device immediately. Follow the manufacturer's recall instructions
Northeast Scientific recalled 141 units of the NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter nationwide in the United States. The device may have breaches in the sterile barrier packaging that could compromise sterility. Hospitals and patients should stop using the device immediately and await instructions from Northeast Scientific Inc. or their clinicians.
Baxter Healthcare recalled 2,304 CLEARLINK System Extension Sets distributed nationwide in the United States. The IV extension set may leak, creating a risk to patients. Stop using the device immediately and follow recall instructions from Baxter or your healthcare provider.
Air Vent recalled electric motors used in gable- and roof-mounted attic fans sold from August 2003 through December 2013. The recall covers five model numbers and centers on a safety cutoff that may short and ignite. Owners should stop using recalled motors and contact Air Vent for a full refund.
CT New Energy Technology recalls CT-ENERGY nc-02 lithium coin battery chargers sold with four rechargeable 2032 batteries and a USB cable. The recall cites potential for serious injury or death from ingested button cells. Consumers should stop using the charger and contact CT New Energy for a full refund, repair, or replacement kit.
Granules Pharmaceuticals recalled 11,909 bottles of Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate Extended-Release Capsules sold nationwide to pharmacies and health care providers. The recall stems from a failure to meet impurities and degradation specifications. Patients taking this prescription should stop using the product and
Boston Scientific recalled 156 units of the Extractor Pro RX Retrieval Balloon Catheter nationwide in the United States after labeling inconsistencies were found. The label misstates whether the skive hole is above or below the balloon. The recall is active as of 2025. Stop using the device immediately and follow manufacturer instructions.
Lulive recalled 12-drawer dressers sold on Amazon after identifying a risk of serious injury or death from tip-over and entrapment. The dressers are white with a metal frame, a wooden top, 12 collapsing fabric drawers, four side pockets and two hooks. They measure about 12 inches by 39 inches by 45 inches and weigh 30 pounds. Consumers should stop using unanchored dressers immediately and contactL
Party Favors recalled four models of lite-up torches and laser pointers due to risk of serious injury or death from swallowed button cell batteries. Imported by MTC Trading. Consumers should stop using the products and seek a full refund.
Granules Pharmaceuticals recalled 11,895 bottles of an extended-release amphetamine product due to failed impurities and degradation specifications. The recall is active nationwide in the United States. The FDA notice lists a high hazard level and urges stop-use and contact with the company or a healthcare provider.
Granules Pharmaceuticals recalled 11,928 bottles of an extended-release amphetamine product. The recall date is 2025-08-28 for Dextroamphetamine saccharate and related salts. The FDA lists the reason as failed impurities and degradation specifications. The recall remains active as of 2025-10-01. Health care providers and patients should stop use and contact the manufacturer for guidance.
Granules Pharmaceuticals recalled 9,917 bottles of mixed-salts amphetamine extended-release capsules nationwide. The recall was issued August 28, 2025 and remains active. The FDA cited failed impurities/degradation specifications as the reason. Healthcare providers and consumers should stop using the product immediately and contact Granules Pharmaceuticals for guidance.
TTI Outdoor Power Equipment recalled 80,000 RYOBI pressure washers after reports of overheating capacitors that can burst. The defect poses a projectile hazard, risking serious injury to users and bystanders. Consumers should stop using these pressure washers immediately and check RYOBI's website for repair instructions.
Granules Pharmaceuticals Inc. recalls 3,384 bottles of Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate Extended-Release Capsules, 5 mg, 100 capsules per bottle, NDC 70010-029-01, Lot GPC250158A, Exp 06-22-2027. The recall concerns failed impurities/degradation specifications. Healthcare providers and consumers should stop using the
Camp USA recalled Nimbus Lock Carabiners sold through various retailers after a safety concern over the automatic closing mechanism. The carabiner's automatic closing mechanism can break and prevent the gate from closing, creating a fall risk. Stop using the recalled carabiners immediately and contact CAMP for inspection, repair or replacement.
Ascend Laboratories, LLC recalls 2,256 bottles of ARIPIPRAZOLE 10 mg tablets distributed nationwide after discovering the product to be superpotent. The recall involves ARIPIPRAZOLE tablets manufactured by Alken Laboratories Ltd. in India and distributed in the United States. The recall date is August 28, 2025, with consumer notification by letter and guidance to stop use.
Siemens Medical Solutions USA recalled 237 MAGNETOM Vida MRI scanners sold worldwide to healthcare providers. The recall cites ice forming in the magnet venting system. A quench could lead to a helium leak into the scanning room. Hospitals must stop using the devices and await manufacturer instructions.