325 recalls tagged with “electronic”.
Philips North America recalled 146 units of Patient Information Center software on December 22, 2025. A software patch modifies Mobile Event Notification filter settings without notifying users. The recall affects units distributed worldwide, including 41 in the U.S.
Wondfo recalled 188 units of Streptococcal A At-Home Self-Test sold nationwide in the United States after regulators found the device was not FDA-cleared. The recall centers on lack of FDA clearance for safety and effectiveness. Consumers should stop using the test immediately and contact Altruan GmbH or their healthcare provider for instructions.
Sanven Technology recalled VEVOR Garment Steamers sold online after a burn hazard was identified. Affected units can leak or spit hot water, and the water tank cap can leak or detach. Consumers should stop using the recalled steamers and request a full refund from Sanven Technology.
TREK recalled four electric bicycles sold through Trek authorized retailers and independent bike shops nationwide and online. The chainring bolts can loosen, causing the chainring to detach and create a fall hazard. Owners should stop riding immediately and contact an authorized Trek dealer for a free repair; Trek provides a $20 in-store credit toward Trek, Electra, or Bontrager merchandise, valid
Intuitive Surgical recalled 2,660 da Vinci S/Si Grasping Retractor Instruments worldwide after increased complaints of broken or frayed grip cables. The devices transmit motion from input disks to the distal tip and are used in robotic surgery. Hospitals and surgical centers should stop using the device immediately and follow recall instructions from the manufacturer.
Intuitive Surgical recalled 2,095 units of the da Vinci S, Si EndoWrist Tenaculum Forceps Instrument distributed nationwide in the United States and in multiple countries after reports of frayed or broken pitch cables. The defect can compromise instrument control during surgery. Hospitals and surgeons should stop using the device immediately and follow recall instructions from Intuitive Surgical.
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.
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.
KTEBO recalled its Writing Tablet Toys sold on Amazon on December 4, 2025. The screw securing the battery compartment containing a button cell battery does not remain attached as required. This creates a risk of ingestion with potential serious injury or death. Consumers should stop using the 2-pack sets immediately and contact KTEBO for a free replacement.
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
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
Olympus Corporation of the Americas is recalling 1,684 ShockPulse-SE Lithotripsy System generators worldwide, including SPL-G models. Investigations found the generator can blink and fail to recognize the transducer, and damage to the transducer plug or generator receptacle may occur. Healthcare providers and patients should stop using the device immediately and follow recall instructions provided
Tesla recalls Powerwall 2 energy storage systems sold through Tesla.com and certified installers nationwide due to fire and burn hazards. The lithium-ion cells can stop functioning during normal use, causing overheating and possibly smoke or flame. Owners should stop using the system and contact Tesla for replacement options.
Lezyne USA recalls two bicycle floor pumps, the Pressure Over Drive and Digital Pressure Over Drive, sold at bicycle stores nationwide and online. The canister can eject from the base when pressurized, posing a serious injury risk. Stop using the recalled pumps and contact Lezyne for a free replacement.
Peloton recalled Original Series Bike+ units with model PL02 and serials beginning with the letter 'T'. The seat post assembly can break during use, creating a fall and injury risk. Consumers should stop using the recalled bikes and contact Peloton for a free repair.
F&F Fine Wines is recalling Kirkland Signature Valdobbiadene Prosecco DOCG bottles sold at Costco due to a laceration hazard from potential breakage. The recall covers UPC 196633883742 and Costco Item Number 1879870. Consumers should stop using recalled bottles immediately and contact Ethica Wines for refund instructions from Costco.
Cepheid recalled 9,880 units of Xpert MTB/RIF GXMTB/RIF-US-10 after testing failed to meet stability criteria. The devices were distributed nationwide in the United States and Puerto Rico. Health care providers and patients should stop using the device immediately and follow the recall instructions.
GET TESTED INTERNATIONAL AB recalled 6 Food Intolerance Test Large units sold nationwide in the US after a premarket approval issue. The device was distributed without premarket approval or clearance. Consumers should stop using the device immediately and contact GET TESTED INTERNATIONAL AB or their healthcare provider for instructions.
GET TESTED INTERNATIONAL AB recalled 166 units of its Candida Test distributed nationwide in the United States. The device was distributed without premarket approval or clearance. Patients and healthcare providers should stop using the device immediately and follow the recall instructions from the manufacturer.
GET TESTED INTERNATIONAL AB recalled 3 units of the Biological Age & Longevity Test distributed nationwide in the United States. The recall concerns distribution without premarket approval or clearance. Consumers should stop using the device and follow the manufacturer's instructions. Contact GET TESTED INTERNATIONAL AB for guidance.