2,056 recalls tagged with “cpsc regulated”.
Pura Scents recalled the Pura 4 Smart Home Fragrance Diffusers sold at retailers on July 24, 2025. The detachable cover contains five magnets and can detach, creating an ingestion hazard for children. Consumers should stop using the diffuser immediately and contact Pura Scents for a free replacement front cover.
Cipla USA Inc. recalls 20,352 packs of Albuterol Sulfate Inhalation Aerosol after failing stability specifications. The defective lots were distributed nationwide in the United States. The issue involves out of specification results in particle size distribution at the 12-month time point. Patients and healthcare providers should stop use and contact Cipla USA for guidance.
Beckman Coulter recalled 685 boxes of MicroScan Neg MIC 56 panels distributed nationwide to U.S. healthcare facilities after contamination was reported in wells. Contamination could lead to unreliable antimicrobial susceptibility and organism-identification results. Health care providers should stop using the panels and follow Beckman Coulter recall instructions immediately.
BMW of North America recalls 2022–2025 i4, 2022–2024 iX, 2023–2024 i7, and 2024 i5 vehicles over software that may shut down the high-voltage system, causing loss of drive power. OTA software updates or dealer service will fix the issue at no cost. Letters to owners begin August 5, 2025.
Taizhou Kangping Medical recalled 3.85 million cartons of BZK Antiseptic Towelettes for external use. The U.S. FDA listing cites lack of assurance of sterility as the reason for recall. Consumers and healthcare providers should stop using this product immediately and contact the manufacturer for guidance.
Ascend Laboratories recalls 8,568 bottles of Amlodipine and Olmesartan Medoxomil tablets due to failed dissolution specifications. The recall covers products manufactured by Alkem Laboratories in India and distributed nationwide in the USA. The defect involves low dissolution results. Stop use immediately and contact Ascend Laboratories for guidance.
Merck Sharp & Dohme LLC recalled 51,320 cartons of Belsomra (suvorexant) tablets after identifying a risk of delayed dissolution. This defect can delay the release of the drug, hindering sleep onset. Consumers and healthcare providers should stop using the product immediately and contact the company for guidance.
Bestway, Intex and Polygroup recall 5 million above-ground pools taller than 48 inches after nine deaths. The recall covers pools whose model numbers are printed on the liner outside the pool. The hazard stems from a compression strap around the pool legs that can create a foothold for a child, enabling access to the water. Stop using the pools immediately and contact the respective brands for a维修
A high-hazard recall is active for Quick Touch Alcohol Prep Pads. 500 cases are affected. The recall covers products from YANGZHOU YULOU PAPER PRODUCTS CO. and AUM Pharmaceuticals. Consumers should stop using immediately and consult healthcare providers for guidance.
Middlefield Original Cheese Cooperative recalled 640 pounds of cheese products due to potential Listeria monocytogenes contamination. The recall covers Monterey Jack and Farmers Cheese in multiple package sizes. Consumers should not eat the cheese and should contact the company for refunds or replacements.
Summa Therapeutics recalled 22 units of the Finesse BTK Multicath Injectable Angioplasty Balloon Catheter sold to healthcare facilities in New Jersey and Florida. The balloon may not meet burst specifications, raising risk during angioplasty. Healthcare providers must stop using the device immediately and follow recall instructions from Summa Therapeutics.
DJO Surgical recalled 927 ALTIVATE reverse wedge glenoid reamer heads distributed nationwide in the United States after concerns that the devices may kick or bind up during use. The issue involves model 804-06-311 and non-sterile stainless steel material. Healthcare providers and patients should stop using the device immediately and contact Encore Medical, LP for instructions.
DJO Surgical recalled 907 units of the ALTIVATE reverse wedge glenoid reamer boss drill 6.5mm sold nationwide in the United States. The device may kick or bind up during use. Healthcare providers and patients should stop using the device immediately and follow recall instructions from Encore Medical, LP.
Tractor Supply recalled three Traveller aluminum loading ramps on July 17, 2025 after determining a fall hazard. The ramps can bend or break under load. Stop using the recalled ramps and seek a full refund from Tractor Supply.
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.
CR Bard recalled 3,670 SureStep Foley Tray System A942216 Foley Catheter Trays nationwide after discovering incorrect inserts. Mislabeling could cause infection or allergic reactions. Healthcare providers should stop using the device immediately and follow recall instructions from the manufacturer.
Five thousand seven hundred three bottles recalled nationwide for microbial contamination with Burkholderia cepacia. DermaRite Industries LLC issued the recall on July 17, 2025. The product is PeriGiene Health Care Antiseptic, 222 mL bottles. Consumers should stop use and contact DermaRite for guidance.
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.
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.