Browse through 3,495 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
ImaCor recalls 45 CLT-010 miniaturized TEE probes nationwide in five states after a production assembly error risks reversed articulation. The device is used with ImaCor model ZHH and Mobile Ultrasound. Stop using the device immediately and follow the manufacturer’s recall instructions.
Rolling Pin Baking Company LLC is recalling 127,680 Dubai Style Chocolate pouches sold through multiple retailers. The recall was announced on Aug. 29, 2025. The product does not declare wheat in the allergen statement. Consumers should not consume the product and contact the company by email for refund or replacement.
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.
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.
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.
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.
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
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
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.
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.
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
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.
DT Swiss recalled carbon road wheels sold aftermarket and on high-end bikes due to a wheel integrity defect that can cause a crash. The recall covers wheels with DT Swiss ID codes of 2740000 or higher. DT Swiss provided a replacement remedy. Consumers should stop riding recalled wheels and contact DT Swiss for a replacement.
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.
Howmedica Osteonics recalled 55 units of EXETER V40 surgical stems distributed in the United Kingdom due to a risk of product mix. Patients may receive the incorrect product, potentially leading to surgical complications. Patients and healthcare providers must stop using the device and follow the manufacturer’s instructions.
Siemens Medical Solutions USA recalled 23 Biograph mMR PET-MRI systems worldwide after detecting an ice blockage in the magnet venting system. In a magnet quench, helium gas may not escape through vent paths, risking rupture of the helium containment and a leak into the scanning room. Hospitals and providers must stop using the device immediately and follow the manufacturer’s recall instructions.
Siemens Medical Solutions USA recalled 30 MAGNETOM Verio Dot MRI systems sold worldwide through hospitals and medical facilities. The ice blockage in the magnet venting system could trap helium during a quench, causing pressure buildup and a potential helium leak into the scanning room. Facilities should stop using the devices immediately and follow the manufacturer’s recall instructions.