2,229 recalls tagged with “stop use immediately”.
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.
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 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 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 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 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 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.
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 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.
Cook Medical recalled 23 units of its Transjugular Liver Access Sets on November 26, 2025. The recall follows concerns that products may have been manufactured out of specification, leading to potential use errors. Healthcare providers and patients should stop using the device immediately and follow recall instructions.
Medline Industries recalled 13,245 homecare beds on November 26, 2025, due to a fire risk from the hand control pendant. The company received 58 reports of sparking, burning, and smoke. Patients and healthcare providers must stop using the beds immediately and follow recall instructions.
Medline Industries recalled 138,412 electric homecare beds on November 26, 2025. Hazardous hand control pendants may overheat and pose a fire risk. The recall follows 58 reports of sparking, burning, and smoking incidents.
Medline Industries recalled 15,581 electric homecare beds on November 26, 2025, due to a fire hazard. The hand control pendant may overheat, posing a risk of fire in rare cases. The recall follows 58 complaints of sparking or burning from the pendant.
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.
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.
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.
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
Beckman Coulter recalled 1,272 UniCel Dxl 600 analyzers on November 26, 2025. A communication issue may prevent the devices from restarting after shutdown, delaying test results. The recall affects multiple countries worldwide.
Outdoor Master recalled two helmet models sold and imported by Outdoor Master after a risk of serious head injury. The recall covers OM-TD BIKE and OM-KSKB helmets. The recall cites noncompliance with positional stability and coverage requirements. Stop using the recalled helmets and contact Outdoor Master for a full refund.