2,715 recalls tagged with “immediate action”.
Philips recalls 670 Azurion 7 B12 X-ray imaging systems after finding the wired foot switch may fail to start imaging. The issue affects 106 US units and 564 in other countries. Hospitals should stop using the device and await manufacturer guidance.
Rising Pharmaceuticals recalls 1,200 Temozolomide 5 mg capsules nationwide after a stability test found out-of-spec impurities. The drug is Rx-only, with NDC 16571-816-51 and lot 1TM0524003A. Stop using immediately and contact a healthcare provider for guidance.
Philips Respironics recalled 113,717 Trilogy Evo O2 home-use ventilators worldwide on March 2, 2026 after determining that using non-pneumatic nebulizers with the device can cause a mismatch between the set tidal volume and the delivered tidal volume. The defect could lead to under- or over-ventilation with serious health consequences. Stop using the device immediately and follow the recall steps.
Civco Medical Instruments recalled 10 eTRAX Needle Sensor 16G units for Aurora Trackers. An inspection and programming error could cause the needle tip position to be misidentified on the user interface. Stop using the device immediately and contact Civco for instructions.
Civco Medical Instruments Co. is recalling 5 eTRAX Needle Sensor 14G units for Aurora Trackers. The recall cites a programming and inspection error that could cause the needle tip position to be misidentified on the user interface. Stop using the device immediately and contact Civco for instructions.
Civco Medical Instruments recalled 18 units of the eTRAX Needle System Starter Kit 16G for Aurora Trackers after an inspection and programming error could cause the needle tip position to be misidentified on the user interface. The defect could lead to incorrect needle guidance during a procedure. Healthcare providers and patients should stop using the device immediately and follow the recall ins
Philips Respironics recalled 113,717 Trilogy Evo ventilators worldwide on March 2, 2026. The recall concerns software Version 1.05.15.00 and the use of non-pneumatic nebulizers with the Trilogy Evo platform. Hospitals and patients should stop using the device immediately and follow recall instructions from Philips Respironics or their healthcare provider.
Philips Respironics recalled 113,717 Trilogy Evo Universal ventilators worldwide on March 2, 2026. The recall cites a condition where using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the delivered tidal volume. Patients and caregivers should stop using the device immediately and contact Philips Respironics or their healthcare provider for instructions.
Philips Respironics recalled 113,717 Trilogy EV300 ventilators sold worldwide through healthcare distributors on March 2, 2026. Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may cause a mismatch between the set tidal volume and the delivered tidal volume. Patients and healthcare providers should stop using the device immediately and follow the recall instructions from the 제조
Philips Respironics recalled 113,717 Trilogy Evo home-use ventilators worldwide after finding the Obstruction Alarm may fail to trigger, potentially delaying alerts by up to four breaths. The devices were distributed nationwide in the United States and internationally. Consumers should stop using the device immediately and follow the manufacturer’s recall instructions.
Philips Respironics recalled 113,717 Trilogy EV300 ventilators sold in the United States and internationally after determining the Obstruction Alarm may fail to trigger within required standards. The alarm can delay alerting caregivers for up to four breaths. Patients and healthcare providers should stop using the device immediately and follow recall instructions from Philips or their clinician.
Civco Medical Instruments recalled 2 eTRAX Needle System Starter Kit 12G units for Aurora Trackers sold to healthcare providers in Ohio, Pennsylvania and Washington. The defect can cause the needle tip position to be incorrectly identified on the user interface. Stop using the device immediately and follow the recall instructions from Civco or your healthcare provider.
Philips Respironics recalls 113,717 Trilogy Evo O2 home-use ventilators in 2026. The Obstruction Alarm may fail to trigger within required standards, delaying warning for airway obstruction for up to four breaths. Stop using the device and follow recall instructions from Philips or your clinician.
Civco Medical Instruments Co. recalled 21 eTRAX Needle Sensors for Aurora Trackers sold to healthcare providers in Ohio, Pennsylvania and Washington. The devices have an inspection and programming error that can cause the needle tip position to be misidentified on the user interface. Clinicians should stop using the devices immediately and follow recall instructions from Civco.
Civco Medical Instruments recalled 20 eTRAX Needle System Starter Kit 18G for Aurora Trackers. An error in inspection and programming of the needle sensor can cause needle tip position to be misidentified on the user interface. Healthcare providers and facilities should stop using the device immediately and follow the recall instructions from the manufacturer.
Five Civco Medical Instruments eTRAX Needle Sensor 12G units for Aurora Trackers are recalled in the United States. The recall cites an inspection and programming error that could misidentify the needle tip position on the user interface. Healthcare providers should stop using the device immediately and follow recall instructions.
Philips Respironics recalled 113,717 Trilogy Evo Universal home-use ventilators sold by multiple retailers after alarms may fail to trigger. The obstruction alarm may not trigger within the required timeframe, delaying warning by up to four breaths. Patients should stop using the device and follow the manufacturer’s recall instructions or contact their healthcare provider for guidance.
Olympus recalls 408 SOLTIVE Premium Laser System units worldwide after a defect in the 24V power supply may render the system inoperable and cause smoke or a burning smell. The issue is contained within the internal console and would self-extinguish. Hospitals should stop using the device immediately and follow recall instructions.
4,611 bottles are recalled nationwide. The product is Savannah Bee Company Honey BBQ Sauce Mustard, distributed to numerous states. The bottle actually contains Honey BBQ Sauce 'Sweet' which contains wheat and soy not declared on the Mustard label. Stop using the product and contact Savannah Bee Company for a refund or replacement.
GE Healthcare recalled 41 SIGNA Premier Whole-Body MRI systems sold worldwide. The devices may have ferrous fittings on the magnet rear instead of brass. If service is performed while the magnet is ramped, the magnetic field could attract the fittings and injure personnel. Hospitals should stop using the devices and follow the manufacturer's recall instructions.