69 recalls tagged with “bedroom”.
EnHomee recalled Fabric 13-Drawer Dressers sold directly by EnHomee Direct due to a tip-over and entrapment hazard. The units do not meet the STURDY Act mandatory standard. Consumers should stop using unanchored dressers and seek a full refund.
B Braun Medical recalled 2,450 SESK pain management trays distributed nationwide. The recall cites a potential mispositioned catheter connector lid, classified as Class II with high hazard. Patients and healthcare providers were advised to stop using the device and follow recall instructions.
Fisher & Paykel Healthcare recalled 51,144 Airvo 2 and myAirvo 2 humidifiers in the United States. The devices may emit an audible alert for less than 120 seconds after power is disconnected. This could delay user awareness to reconnect power and lead to oxygen desaturation. Patients and healthcare providers should stop using the device and await manufacturer instructions.
In My Jammers recalls children's button-up flare pajama sets sold online after the company violated mandatory flammability standards. The recall, active as of Sept. 11, 2025, involves sets in multiple prints and sizes. Parents should stop using them and seek a full refund or store credit.
Olympus Corporation of the Americas confirms a Class I recall of the BRONCHOFIBERSCOPE BF TYPE PE2. The recall covers 2 units in the US and 4,289 units outside the US. Updated IFU guidance aims to clarify safe use with laser, argon plasma coagulation and high-frequency therapy equipment.
Olympus Corporation of the Americas reports an active recall for the BRONCHOVIDEOSCOPE BF-1TH1100. The recall concerns additional IFU updates for safe use with laser, argon plasma coagulation, and high-frequency therapy equipment. The company urges stopping use and following recall instructions.
Boston Scientific recalled 172 units of the CXR Preconnect with TENACIO Pump with InhibiZone worldwide. The recall was initiated on 2025-09-11 and remains active as of 2025-10-22. The devices can experience inflation and/or deflation performance issues. Healthcare providers should stop using the devices and follow manufacturer instructions for recall remediation.
URMYWO recalled its baby loungers on 2025-09-04 after reports of suffocation and fall hazards. The recall targets URMYWO loungers style grey feather sold via Amazon by Pomona. The devices fail to meet infant sleep standards due to short side walls and excessive pad thickness. Consumers should stop using the loungers and request a full refund.
Baxter Healthcare recalled 136,512 CLEARLINK System Solution Set DUO-VENT IV sets distributed nationwide in the United States after detecting a leak risk. The Luer Activated Valve design may leak, potentially compromising IV administration. Hospitals and patients should stop using the device immediately and follow Baxter recall instructions.
Northeast Scientific recalled 561 units of NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. The recall covers all lots within shelf life ending before August 29, 2026. The hazard is breaches in sterile barrier packaging that could compromise sterility. Stop using the device and follow manufacturer instructions for return or replacement.
ImaCor recalls 45 CLT-010 miniaturized TEE probes nationwide in five states after a production assembly error risks reversed articulation. The device is used with ImaCor model ZHH and Mobile Ultrasound. Stop using the device immediately and follow the manufacturer’s recall instructions.
DT Swiss recalled carbon road wheels sold aftermarket and on high-end bikes due to a wheel integrity defect that can cause a crash. The recall covers wheels with DT Swiss ID codes of 2740000 or higher. DT Swiss provided a replacement remedy. Consumers should stop riding recalled wheels and contact DT Swiss for a replacement.
Lulive recalled 12-drawer dressers sold on Amazon after identifying a risk of serious injury or death from tip-over and entrapment. The dressers are white with a metal frame, a wooden top, 12 collapsing fabric drawers, four side pockets and two hooks. They measure about 12 inches by 39 inches by 45 inches and weigh 30 pounds. Consumers should stop using unanchored dressers immediately and contactL
Siemens Medical Solutions USA recalled 71 MAGNETOM Lumina MRI systems worldwide, including US and 50+ countries, due to ice blockage in the magnet venting system that could cause a helium leak during a quench.
Sunrise Creamery Monterey Jack Cheese with Dill Pickles is recalled by Middlefield Original Cheese Cooperative after FDA findings indicate potential Listeria monocytogenes contamination. The recall covers two SKUs in 6 oz and 1.25 lb sizes, distributed to Ohio, Pennsylvania, Wisconsin and Texas. Consumers should discard affected cheese and contact the cooperative for refund or replacement.
FDA recalls READYPREP PVP, povodone-iodine 10% topical antiseptic. Medline Industries issued the nationwide recall. Subpotent drug is the reason. Consumers should stop using the product immediately.
B. Braun Medical Inc. recalls 47,148 containers of 0.9% Sodium Chloride Injection USP nationwide after detecting particulate matter. The Class I recall affects bottles with NDC 0264-7800-09. Stop using and contact providers for guidance.
Philips recalled 3 Ingenuity CT Family Brazil systems, Model 728325, distributed worldwide, including the United States. A ball screw misalignment after a replacement may cause the patient support table to descend to the lowest position. Hospitals and clinicians should stop using the device and follow Philips recall instructions.
Philips North America LLC is recalling 181 CT systems worldwide, including Brilliance CT 40 Channel 728235, Brilliance CT 64 Channel 728231, and Ingenuity Flex 728317. The patient support couch may descend to the lowermost position after a replacement. Hospitals and imaging centers should stop using the devices immediately and await recall instructions.
H & N Group recalled 17,214 cases of frozen shrimp distributed to East Coast retailers after potential Cs-137 contamination. The product was manufactured under insanitary conditions. Consumers should not eat this product and should contact H & N Group for refund or replacement by telephone.