2,756 recalls tagged with “immediate action”.
RaySearch Laboratories AB recalled its RayStation/RayPlan software on November 28, 2025, due to potential inaccuracies in radiation dose calculations. The issue affects certain Regions of Interest (ROIs) and could lead to incorrect treatment planning. Healthcare providers and patients should stop using the software immediately.
Advanced Bionics recalled 2 Sky CI M90 behind-the-ear sound processors on 2025-11-27. The packaging label does not match the included product. Consumers should stop using the device and follow manufacturer instructions.
Ikuso recalled its safety pressure-mounted gates after regulators found a design flaw that could let a child’s torso pass through the opening. The white steel gates are sold in two sizes and labeled with model numbers Door-Gen1-123 and Door-Gen1-159. The recall violates the mandatory standard for expansion gates and enclosures. Consumers should stop using the gates and request a full refund by U.S
Medline Industries recalled 32 units of its Deluxe Pre Op Kits on November 26, 2025. The recall stems from customer complaints about check valve components potentially sticking in open or closed positions. Patients and healthcare providers must stop using these devices immediately and follow recall instructions.
KingPavonini recalled six adult portable bed rails sold on Amazon after determining the product poses a risk of serious injury or death from entrapment and asphyxiation. The recall cites a failure to meet mandatory standards and missing hazard warning labels. Consumers should stop using the recalled bed rails immediately and contact KingPavonini for a refund or free replacement.
Macardac Products recalled Macardac baby loungers sold on Amazon after safety concerns. The loungers have sides that are too low and openings at the foot that are wider than allowed. The issues can lead to entrapment or fall injuries. Parents should stop using the loungers immediately and contact Macardac for a full refund.
Medline Industries recalled Medline Kits containing B. Braun IV Administration Sets on November 26, 2025. The recall follows customer complaints about check valve components becoming stuck. Affected kits include the AN01 Carotid Anesth Kit-LF, SKU PHS972096014B.
Medline Industries recalled 12 IV administration kits on November 26, 2025. The kits may contain defective check valve components that can become stuck. Patients and healthcare providers should stop using these devices immediately.
Medline Industries recalled 96 IV administration sets on November 26, 2025, due to a defect in the check valve. The defect can cause the valves to become stuck, posing a high risk for patients. Users should stop using the products immediately and follow the recall instructions.
Medline Industries recalled 1,725 IV Administration Sets on November 26, 2025. The recall affects multiple kits due to potential valve malfunctions. Consumers and healthcare providers must stop using these devices immediately.
Medline Industries recalled 3,045 IV administration kits on November 26, 2025. The recall affects several Medline kits due to potential malfunction of check valve components. Patients and healthcare providers should stop using these devices immediately.
Medline Industries recalled 16 units of IV Administration Sets on November 26, 2025. Customers reported check valve components may become stuck, posing a risk during use. Healthcare providers should stop using these devices immediately and follow recall instructions.
Medline Industries recalled 33 units of IV Administration Sets on November 26, 2025. The recall follows customer complaints about check valve components potentially becoming stuck. This defect poses a high risk to patient safety and requires immediate action from healthcare providers.
Medline Industries recalled 338 IV Administration Sets on November 26, 2025. The recall stems from complaints about malfunctioning check valve components. Patients and healthcare providers must stop using these devices immediately.
Walmart is recalling Ozark Trail Tabletop 1-Burner Butane Camping Stoves sold at Walmart. The recall covers model BG2247A1. The stoves can explode or catch fire, posing burn and fire hazards. Consumers should stop using recalled stoves immediately and return them to any Walmart store for a full refund.
McLee Creations recalled the MyOnlyStyler Root Booster Hair Dryers. The recall involves units printed with MOS-22 on the back of the handle. The product is white with black bristles and measures 12 inches long by 1.75 inches wide. The manufacturer cautions the device lacks immersion protection. Consumers should unplug and stop using recalled dryers and file for a full refund through the recall web
Alinux recalled its baby loungers sold on Amazon by Winkids after safety concerns. The foam pad and padded bumpers with a cloth cover and a ribbon tie create openings and low sides that can trap an infant or allow a fall. Consumers should stop using the loungers and email alinuxrecall@163.com for a full refund.
Rotinyard recalled convertible high chairs sold on Amazon after identifying fall and head entrapment hazards. The chairs were sold without the required attached restraint system and the opening between the seat and tray can trap a child’s head. Consumers should stop using the recalled chairs and contact Rotinyard for a full refund.
Vivohome recalled adult portable bed rails due to a risk of entrapment and asphyxiation. The recall covers models VH1316-WC and VH1316-WH. The rails measure about 36.6 inches long, 16.1 inches wide and 15.7 inches high and have a wooden or metallic top bar with a red release button that can collapse. Stop using the recalled rails and contact Vivohome for a full refund.
Medline Industries recalled 22,565 Full Electric Low Basic Homecare Beds on November 26, 2025, due to a fire risk. The recall affects beds labeled with REF MDR107003ELO following 58 reports of overheating hand control pendants. Consumers should stop using the beds and follow recall instructions immediately.