2,056 recalls tagged with “cpsc regulated”.
RaySearch Laboratories recalled a radiation therapy treatment planning system on November 28, 2025. The recall affects 10 units of RayStation software versions 11.0.0, 11.0.1, 11.0.3, and 11.0.4. The system may inaccurately calculate radiation doses for certain Regions of Interest, posing a high risk to patients.
RaySearch Laboratories recalled its RayStation and RayPlan software on November 28, 2025. The software fails to invalidate calculated radiation doses for certain Regions of Interest, posing a high risk to patients. Healthcare providers must stop using the device and follow recall instructions immediately.
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.
Medline Industries recalled 373,392 homecare beds on November 26, 2025, due to a fire hazard. The hand control pendant can overheat, causing sparking or burning. The recall affects models MDR107002E and MDR107002E-4 sold in the U.S. and Canada.
Wayfair sold the Ebern Designs Ojaswi 12-Drawer Dressers from January 2025 through October 2025 for about $75. The recall covers models HD011BL-SL and HD011WH-SL. The dressers measure 39 inches by 43 inches by 12 inches and weigh about 31.7 pounds. They can tip over if not anchored to a wall, posing a risk of serious injury or death to children. Consumers should stop using the recalled dressers if
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.
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.
Sofoliana and Glotika baby loungers sold on Amazon by Bosen US are recalled due to risk of serious injury or death. The recall cites low sides and wide foot openings that can cause entrapment and falls. Consumers should stop using the loungers immediately and contact Bosen US for a full refund.
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.
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 633 units of IV administration sets on November 26, 2025. The recall follows complaints that check valve components may become stuck, posing a high risk to patient safety. Healthcare providers and patients must stop using affected products 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 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 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 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 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.