1,120 recalls tagged with “electrical hazard”.
iStore recalled its Magnetic Wireless Power Bank, 5000 mAh, imported by Tomauri. The lithium-ion battery can overheat and ignite while charging. Only IST-09991/W05 units are affected; consumers should stop using the recalled power bank and return it for a full refund.
VIVI recalled 36-volt lithium-ion batteries included with certain VIVI brand e-bikes sold by VIVI. The batteries can overheat and pose fire and burn hazards. Stop using affected e-bikes immediately and contact VIVI for a free replacement battery and charger.
Quest International recalls 376 Measles IgM ELISA kits nationwide in Utah, Texas and Arizona after discovering the product lacks premarket approval or clearance. The high-risk health device carries a Class II designation. Stop using the device immediately and follow manufacturer recall instructions.
DermaRite Industries’ DermaKleen antiseptic lotion soap is recalled nationwide after contamination with Burkholderia cepacia. The Class I recall covers 11,321 bag-in-box units sold nationwide. Consumers are urged to stop using the products and contact the company for guidance.
Babyletto recalled its Kiwi Electronic Recliner and Glider chairs due to an overheating USB module. The USB module can overheat and spark, posing an overheating hazard. Consumers should stop using the recalled chairs and contact Babyletto for a free repair kit.
4,300 SureStep Foley Tray System Bardex I.C. Complete Care catheter tray units are recalled nationwide by C.R. Bard. The trays may contain incorrect inserts, creating a risk of infection or an allergic reaction. Healthcare providers and patients should stop using the device and follow Bard’s recall instructions.
C.R. Bard Inc. recalls 4,300 SureStep Foley Tray System Lubri-Sil I.C. Complete Care infection control Foley catheter trays nationwide in the United States. The trays may contain incorrect inserts that misrepresent material composition. The mismatch could trigger infections or allergic reactions. Health care providers should stop use and follow recall instructions immediately.
DermaRite Industries recalled 249 bottles of DermaSarra External Analgesic on July 17, 2025 due to microbial contamination. The product, sold nationwide, carries NDC 61924-189-08 and Lot 40187.2 with an expiration date of February 2026. Consumers should stop using the product immediately and contact DermaRite for guidance.
Stryker Communications recalls 40 surgical light systems nationwide after reports of stress lines in the powder coating. The devices include CH00000001 and the SLX to Oculan NFC Upgrade Kit, P60034. The recall is active as of July 15, 2025. Patients and healthcare providers should stop using the devices immediately and follow manufacturer recall instructions.
Dearlomum retractable mesh safety gates sold on Amazon by Signbaby are recalled. The gates violate federal expansion gate standards because a child's torso can fit through the base opening, creating a risk of serious injury or death from entrapment. Stop using the recalled gates immediately and contact Signbaby for a full refund; disassemble, destroy the mesh, and email a photo to regcards.team@gm
Walmart recalls Ozark Trail 64 oz stainless steel insulated water bottles sold at Walmart due to a lid ejection hazard. The one-piece screwcap lid can forcefully eject when opened after liquids are stored inside, creating a risk of impact and laceration. Stop using the recalled bottles and contact Walmart for a full refund.
Boothwyn Pharmacy recalls 8 vials of Fluorescein 2% Ophth 3 mL nationwide after a subpotent drug finding. The recall was issued July 9, 2025 and remains active.
Boston Scientific Neuromodulation recalls 25,260 Vercise DBS devices worldwide over wire breaks in rechargeable implantable pulse generators. The defect can prevent stimulation and trigger device removal. Patients should contact their provider for guidance and stop using affected devices immediately.
Medline Industries recalled 6,669,874 units of Alcohol Prep Pads nationwide after detecting subpotent isopropyl alcohol. The pads were distributed nationwide. The recall is classified as Class II with a high hazard level. Consumers and healthcare providers should stop using the product immediately and contact Medline for guidance.
CURAD Alcohol Prep Pads recalled nationwide after tests found isopropyl alcohol levels subpotent. Medline Industries is the maker listed on recall documents. The issue concerns diluted potency below labeled concentration. Stop using immediately and contact Medline for guidance.
Tandem Diabetes Care recalls 19 units of the t:slim X2 insulin pump with interoperable technology distributed internationally, including Israel. An app defect occurs when the phone uses a right-to-left language and can cause app-pump pairing problems and graphical defects. Patients should stop using the device immediately and follow the manufacturer’s recall instructions.
North American Rescue recalled 552 units of the JETT device, used for occlusion of blood flow to the lower limbs, due to a manufacturing defect that may compromise structural integrity and performance. The recall covers multiple kits distributed worldwide, including U.S. states and several international countries. Stop using the device immediately and await recall instructions from the company or
CHETAK NEW YORK LLC recalled 5,232 packets of Deep Sprouted Mat 16 oz distributed to California, New Jersey, Illinois, Florida and Texas after tests found Salmonella. The recall class is I with a high hazard level. Consumers should not consume the product and should seek refund or replacement by email.
Ford Motor Company recalls certain 2025 Expedition and Navigator vehicles due to a passenger-side frontal air bag that may deploy with excessive force. Dealers will replace the passenger side air bags at no charge. Owner notification letters were mailed August 8, 2025.
GM recalls 2024-2025 Chevrolet Blazer EVs due to a rear parking brake wiring harness that may corrode or become damaged. The defect can cause unintended parking brake activation or loss of function, increasing crash risk. Dealers will inspect and reroute the harness, install anti-abrasive tape, and replace damaged harnesses at no cost. Owner notices mailed October 1, 2025. Contact Chevrolet at 1-[