2,756 recalls tagged with “immediate action”.
Philips North America is recalling 1,913,441 IntelliVue MP60 patient monitors. The monitors may fail to alarm as designed. Hospitals and clinics using MP60 units should stop using the devices and follow the recall instructions.
Philips recalled 1,913,441 IntelliVue MX600 patient monitors distributed worldwide after reports that the devices did not alarm. The defect could prevent alarms that alert clinicians to patient distress. Hospitals and clinicians should stop using the devices immediately and follow the recall instructions from Philips North America LLC.
Philips North America LLC recalled 1,913,441 IntelliVue Multi Measurement Server X2 M3002A monitors sold to hospitals and healthcare facilities worldwide after reports the devices could fail to alarm. The defect could delay critical warnings for patients. Healthcare facilities should stop using the devices immediately and follow recall instructions from Philips or their healthcare provider.
Philips North America recalled 1,913,441 IntelliVue Patient Monitors on October 31, 2025. The monitors may fail to alarm, posing serious risks to patients. Users must stop using the device immediately and follow the manufacturer's instructions.
Trifecta Pharmaceuticals recalled 33,000 containers of Globe Zinc Oxide Ointment on October 31, 2025, due to cGMP deviations. Consumers should stop using the product immediately to avoid potential risks. Healthcare providers are advised to contact the company for further guidance.
STRYKER recalled 39,148 NICO Myriad Handpieces sold worldwide due to latex in packaging that could trigger allergic reactions. The latex-containing tape secures components within packaging. Healthcare providers and patients should stop using the device immediately and follow the recall instructions from Stryker.
Stryker recalled 39,148 NICO BrainPath BrainPath Shephard's Hook devices distributed worldwide through multiple healthcare providers. latex-containing tape in packaging is the defect, despite latex-free labeling. Stop using the device now and follow recall instructions from Stryker or your healthcare provider.
Philips recalls 1.913 million IntelliVue MP20 patient monitors worldwide because the devices may fail to alarm. The issue could prevent critical alerts from sounding. Hospitals should stop using the monitors immediately and follow Philips recall instructions.
Philips North America recalled 1,913,441 IntelliVue Patient Monitors on October 31, 2025. The monitors may fail to alarm, posing a serious risk to patient safety. Healthcare providers and patients should stop using the device immediately and follow recall instructions.
Cipla USA recalled 4,438 cartons of Phytonadione Injectable Emulsion on October 31, 2025. The product failed stability specifications, raising concerns about its safety. Consumers and healthcare providers must stop using the product immediately and seek guidance.
Philips North America is recalling 1,913,441 IntelliVue MP2 patient monitors worldwide. The devices may fail to alarm when critical conditions arise. Hospitals should stop using the monitors and follow Philips recall instructions.
Dyrnarex Corporation recalled 1,560 containers of Dynashield Skin Protectant on October 31, 2025. The product may not meet current Good Manufacturing Practice standards. Consumers should stop using the product immediately and seek guidance from healthcare providers.
Philips North America LLC recalled 1,913,441 IntelliVue MP80 patient monitors distributed worldwide to hospitals after reports the devices did not alarm. The defect could prevent alarms from sounding in critical patient situations. Healthcare facilities should stop using the monitors and follow recall instructions from the manufacturer.
Dynarex Corporation recalled 2,400 containers of Wecare Calasoothe on October 31, 2025, due to cGMP deviations. The recall affects the 4 oz ointment, as it may not meet safety standards. Consumers should stop using the product immediately and consult their healthcare providers.
The Kroger Co. recalls Halloween-themed Skeleton Wax Candles sold at Kroger stores due to a fire hazard. The candle contains flammable ornaments that create a burn risk. Consumers should stop using the candle immediately and return it to any Kroger store for a full refund.
Milwaukee Tool recalls its M18 FUEL 12" and 14" Top-Handle Chainsaws. The recall covers catalog number 2826-20 with a serial break identified by the 4th digit as 'A'. The chain brake may fail to activate, creating a laceration hazard. Consumers should stop using the recalled chainsaw immediately and contact Milwaukee Tool for a free repair.
Modera recalled its Pack N Play Play Yard Mattresses sold at multiple retailers after a potential entrapment risk. The products may not fit play yards properly, creating dangerous gaps. Stop using the recalled mattresses and contact Modera for a full refund.
Olympus Corporation of the Americas recalled 7,803 HX-400U-30 single‑use ligating devices distributed nationwide in the United States. The ligation loop may fail to release or detach. Hospitals and clinics should stop using the device immediately and follow the recall instructions from Olympus or their healthcare providers.
WLIVE expanded its recall to include 16-drawer fabric dressers sold on Amazon. The hazard is tip-over and entrapment risk that can cause serious injury or death to children. Stop using the recalled dressers immediately if not anchored to a wall and contact WLIVE for a full refund.
Avenco and Novilla mattresses marketed by PT Champion are recalled for a serious fire risk. The recall covers models in 6, 10, 12 and 14 inches of thickness across twin to king sizes. Consumers should stop using these mattresses immediately and contact PT Champion for a free fitted cover or repair options.