2,756 recalls tagged with “immediate action”.
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.
ORL Labs, LLC recalled 570 bottles of ORL Kids Mouthwash, Bubblegum Flavor on December 8, 2025. The recall stems from violations of current Good Manufacturing Practices (cGMP). The product was distributed only in Arizona and poses potential safety risks for children.
Philips recalled 990 Azurion Systems on December 8, 2025, after nine software issues were identified. The defects may cause loss of X-ray functionality, system restarts, and other operational failures. Healthcare providers must stop using the devices immediately.
Sam Dry Fruits & Nuts Enterprises recalled 32,610 pounds of pistachio meats on December 8, 2025. The recall stems from potential Salmonella contamination. Consumers should not consume the product and seek a refund.
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.
Beckman Coulter recalled 34,451 units of its LDL Cholesterol OSR6x96 assay on December 8, 2025, due to significant performance interference. The recall affects multiple states in the U.S. and several countries internationally. Affected products may provide inaccurate LDL cholesterol readings, posing health risks to patients.
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.
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.
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.
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.
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.
Bharat Bazar recalled 180 packages of SOMA Kitchen Natural Asafoetida on December 5, 2025, due to undeclared wheat. The product, sold in 4-ounce containers, poses a high risk of allergic reactions for those with wheat allergies. Consumers should stop using the product immediately and contact Bharat Bazar for refunds.
Fresh & Ready Foods recalled 200 units of its Evergreen Refreshments brand Ready to Eat Tacos on December 5, 2025. The product may contain foreign material posing a health risk. Consumers should not eat the product and seek a refund.
LimFlow recalled 33 units of its Vector model VT-US-23 on December 5, 2025, due to incorrect expiration dates. Patients and healthcare providers should stop using this device immediately. The recall affects distribution across 14 states and the District of Columbia.
Fresh & Ready Foods recalled 62 units of Spicy Egg Potatoes Cheese Tacos on December 5, 2025. The product may contain foreign material posing a health risk. Consumers should not eat the tacos and seek refunds immediately.
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.