2,229 recalls tagged with “stop use immediately”.
Steris recalled 22 AMSCO 7053HP Washer/Disinfectors on November 19, 2025, due to a risk of electrical arcing. The issue arises from a wire connected to the electrical box that may shift from its intended position. Users must stop using the device immediately and follow recall instructions.
Glenmark Pharmaceuticals recalled 672 bottles of Nebivolol Tablets on November 18, 2025, due to cross-contamination. The 20 mg tablets, prescribed for hypertension, may pose health risks. Consumers should stop using the product and seek guidance from healthcare providers.
AGFA Healthcare recalled 35 Digital Radiography X-Ray systems on November 18, 2025, due to a risk of exceeding safe radiation levels. The recall affects systems distributed nationwide in the U.S. Users must stop using the device immediately and follow manufacturer instructions.
ETAC A/S recalled 64 units of Molift 2-point sling bars on November 17, 2025. A defect in the mounting bolt can lead to failure during use. This poses serious risks for users relying on the device for mobility assistance.
Intuitive Surgical recalled 12 Da Vinci 5 surgical consoles on November 17, 2025. A software error may cause loss of user interface content on external monitors. Healthcare providers must stop using the devices immediately.
Molift recalled 71 Mover 300 mobile hoists on November 17, 2025, due to a potential bolt failure. The defect can lead to limited mobility, posing a high risk to users. Affected models include M1501, M1502, M1504, among others.
ETAC A/S recalled 25 units of the Molift 4-point sling bars on November 17, 2025, due to a defect that can lead to improper functionality. The issue stems from a bolt that may break during assembly and load testing, posing a high risk during use. This recall affects products distributed worldwide, including the United States and several European countries.
Sophysa recalled 105 units of the Pressio 2 ICP Monitoring System on November 17, 2025, after receiving customer complaints regarding unexpected rebooting. This defect poses a high risk for patients relying on the device for monitoring intracranial pressure. Users should stop using the device immediately and follow the manufacturer's instructions.
ETAC A/S recalled 95 Molift Mover 205 devices due to a serious defect. The lifting bar bolt can break during use, posing a high risk of injury. Customers should stop using the product immediately and contact the company for further instructions.
Prime Food Processing recalled 2,243 cases of Lava Bun with Green Tea Flavor sold across 33 states. Milk is not declared in the contains or ingredient statement. Consumers should not consume this product and contact Prime Food Processing for refund or replacement.
Prime Food Processing LLC recalls Lava Bun with Salted Egg Yolk sold at multiple retailers nationwide after undeclared milk was found in the product. The issue centers on missing milk declarations in the Contains and ingredient statements. Consumers should not eat the product and should contact Prime Food Processing for a refund or replacement.
Cipla USA, Inc. recalled 15,744 bottles of Cinacalcet Hydrochloride Tablets on November 14, 2025. The recall follows the discovery of a nitrosamine impurity exceeding acceptable daily intake limits. Consumers should stop using the product immediately and consult healthcare providers.
Olympus Corporation of the Americas is recalling 1,684 ShockPulse-SE Lithotripsy System generators worldwide, including SPL-G models. Investigations found the generator can blink and fail to recognize the transducer, and damage to the transducer plug or generator receptacle may occur. Healthcare providers and patients should stop using the device immediately and follow recall instructions provided
Olympus Corporation of the Americas recalls 602 ShockPulse-SE Lithotripsy System reusable probes worldwide to hospitals. The recall cites a blinking generator that may fail to recognize the transducer and damage the transducer plug or generator receptacle. Hospitals and patients should stop using SPL-SR probes immediately and follow manufacturer recall instructions.
Olympus Corporation of the Americas is recalling 1,082 ShockPulse Lithotripsy System SPL-S single-use probes worldwide. Investigations found the device’s generator may blink and fail to recognize the transducer, risking damage to the transducer plug or generator receptacle. Hospitals and clinics should stop using the device immediately and follow the recall instructions from Olympus.
American Nuts recalls 2,700 units of Dry Roasted Macadamia Nuts, Unsalted Halves distributed to two consignees in Hawaii after a potential Salmonella contamination. The product has UPC 8 60011 44301 8 and Lot Code 307HMNC25L3. Stop consuming the product and contact American Nuts, LLC by telephone for a refund or replacement.
Tesla recalls Powerwall 2 energy storage systems sold through Tesla.com and certified installers nationwide due to fire and burn hazards. The lithium-ion cells can stop functioning during normal use, causing overheating and possibly smoke or flame. Owners should stop using the system and contact Tesla for replacement options.
Belkin is recalling its MMA008 charging stand and BPB002 and PB0003 power banks sold at multiple retailers due to a fire and burn hazard. The lithium-ion battery can overheat. Consumers should stop using the recalled devices immediately and contact Belkin for a full refund or store credit.
Trek and Electra recall certain bicycles and replacement rear wheels sold by Trek authorized retailers and Trek.com due to a crash hazard. The coaster brakes can fail to engage, increasing the risk of loss of rider control. Consumers should stop riding recalled bikes, check serial numbers starting with WTU located under the bottom bracket, and contact a Trek or Electra dealer to schedule a free, 3
Shantou Chenghai Xingzigu Toy Industry recalled Bettina Doll Sets sold on Amazon after finding the unicorn’s battery compartment is easily accessed by children. Button cell batteries can cause serious injuries or death if swallowed. Stop using the recalled toys and request a full refund by emailing bettinaaftersales@outlook.com.