2,229 recalls tagged with “stop use immediately”.
Heraeus Medical GmbH recalled PALACOS MV+G pro 40 and MV+G pro 80 bone cement on December 9, 2025. The recall follows complaints about ampoule breakage, which can prevent proper cement formation. This issue could jeopardize patient safety during medical procedures.
Heraeus Medical GmbH recalled PALACOS R pro 40 and R pro 80 bone cement on December 9, 2025. The recall follows multiple complaints of ampoule breakage affecting product usability. Healthcare providers must stop using the product immediately.
Hyundai recalls 2025 IONIQ 5 EVs for improperly tightened rear suspension alignment adjustment bolts. The issue risks loss of stability control and potentially a crash. Hyundai will repair free of charge, with owner notices mailing November 10, 2025. VINs are searchable on NHTSA.gov as of September 13, 2025.
Heraeus Medical GmbH recalled PALACOS R+G pro 40 and 80 bone cements on December 9, 2025. The recall follows multiple reports of ampoule breakage that prevent proper use of the product. Patients and healthcare providers must stop using the affected devices immediately.
Hyundai Motor America recalls 2023-2025 IONIQ 6 electric vehicles due to a charging port door panel that may detach. Dealers will apply adhesive as the remedy. Owner letters begin November 10, 2025. VINs searchable on NHTSA as of September 13, 2025.
Heraeus Medical GmbH recalled PALACOS MV pro 40 and MV pro 80 bone cement on December 9, 2025. The recall follows numerous complaints about ampoule breakage. This defect can prevent proper cement dough formation, rendering the product unusable for patients.
Intuitive Surgical recalled 2,095 units of the da Vinci S, Si EndoWrist Tenaculum Forceps Instrument distributed nationwide in the United States and in multiple countries after reports of frayed or broken pitch cables. The defect can compromise instrument control during surgery. Hospitals and surgeons should stop using the device immediately and follow recall instructions from Intuitive Surgical.
Intuitive Surgical recalled 2,660 da Vinci S/Si Grasping Retractor Instruments worldwide after increased complaints of broken or frayed grip cables. The devices transmit motion from input disks to the distal tip and are used in robotic surgery. Hospitals and surgical centers should stop using the device immediately and follow recall instructions from the manufacturer.
Securitas Healthcare recalled 5,627 Arial 900 MHz Call Stations on December 8, 2025. A firmware issue may prevent low battery alerts from being transmitted, posing a risk. Affected devices were sold worldwide, including the US and Canada.
Securitas Healthcare recalled 1,898 units of the Arial 900 MHz Call Station on December 8, 2025. A firmware issue may prevent low battery alerts, posing a risk of battery failure. Users should stop using the device immediately and follow recall instructions.
ORL Labs recalled 1,458 containers of ORL Kids Natural Toothpaste, Bubblegum Flavor, on December 8, 2025. The recall follows cGMP deviations that could pose health risks. Consumers should stop using the product immediately.
IMRIS Imaging recalled 122 Head Fixation Devices on December 8, 2025. A torque screw may crack or separate, posing serious risks during surgical procedures. Healthcare providers must stop using the device and follow recall instructions immediately.
Chrysler recalls 2024-2025 Dodge Charger vehicles sold through Dodge and Chrysler dealerships nationwide. The exterior pedestrian alert amplifier software may be missing, preventing the warning sound from emitting. Dealers will update the software free of charge after owner notices mailed on June 26, 2025.
Honda is recalling 2021-2025 Acura TLX, 2023-2025 Acura MDX, and 2023-2025 Honda Pilot vehicles over a brake pedal pivot pin that may loosen. The defect can shift the pedal, reducing braking ability. Dealer repairs are free. Honda notified owners on July 29, 2025. Contact Honda at 1-888-234-2138.
Keurig Green Mountain recalled 960 cartons of McCafe Premium Roast Decaf Coffee K-Cup Pods on December 6, 2025. The product is inaccurately labeled as decaf but may contain caffeine. Consumers in CA, IN, and NV should not consume the pods and seek refunds.
INIU recalled 10,000mAh portable power banks sold on Amazon after identifying a fire risk from overheating. The recall covers BI-B41 models with serial numbers 000G21, 000H21, 000I21 and 000L21. Consumers should stop using the recalled power banks immediately and contact INIU for a full refund.
Meridian Bioscience recalled 211 units of the Revogene C. difficile diagnostic assay on December 5, 2025. Users may experience false-negative results due to a decline in performance over time. Patients and healthcare providers must stop using the device immediately.
Beaver-Visitec International recalled five units of the OME6000U Laser and Endoscopy System on December 5, 2025. The recall stems from a manufacturing deviation where ferrites required for the USB cable were not installed. This omission poses a high electrical hazard risk to patients and healthcare providers.
Siemens Medical Solutions USA recalled LUMINOS Lotus Max and Luminos dRF Max systems on December 5, 2025. The recall affects systems with software version VF11 and involves a potential collimation error. Healthcare providers and patients must stop using the devices immediately.
Merit Medical Systems recalled 2,192 units of its Custom Manifold Kit on December 4, 2025. The inflation device handle may detach from the syringe during procedures. This poses a significant risk to patients and healthcare providers.