1,716 recalls tagged with “cpsc regulated”.
Zap Surgical Systems recalled 17 ZAP-X Radiosurgery Systems on July 25, 2025. A software defect may cause the collimator to collide with patients during operation. Healthcare providers should stop using the device immediately.
Home Health US recalled 4,661 sterile lancets on July 25, 2025. The recall stems from incorrect or missing Unique Device Identifier (UDI) codes. Affected products were distributed nationwide through Amazon.
LIVACTI recalled retractable safety gates on July 24, 2025, due to serious entrapment hazards. The gates can pose a risk of injury or death to children. Consumers should stop using them immediately and seek refunds.
Diamond G Forest Products recalled turpentine bottles on July 24, 2025, due to a risk of child poisoning. The 4-ounce glass bottles lack child-resistant packaging, violating safety standards. The recall affects an unspecified number of bottles sold nationwide.
Minongad recalled LED gloves model ST01 on July 24, 2025, due to a serious battery ingestion risk. The gloves contain lithium coin batteries that can be accessed by children, posing a high danger of serious injury or death. Consumers should stop using the gloves and return them for a full refund.
Cipla USA, Inc. recalled 20,352 packs of Albuterol Sulfate inhalation aerosol on July 24, 2025. The recall follows out-of-specification results in particle size distribution during stability testing. Consumers must stop using the product immediately.
Everpress Juice recalled spicy lemonade on July 24, 2025, due to under-processing that may lead to harmful bacteria. This recall affects consumers in 14 states including California and Texas. The product poses a high health risk and should not be consumed.
Everpress Juice recalled its upbeat product on July 24, 2025, due to under-processing potentially exposing consumers to pathogenic bacteria. The recall affects consumers across 15 states, including California and Texas. No injuries or illnesses have been reported, but the risk remains high.
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.
Everpress Juice recalled Pineapple Mint Juice on July 24, 2025, due to potential contamination with pathogenic bacteria. This under-processed product poses a serious health risk to consumers. The recall affects multiple states including California and Texas.
Everpress Juice recalled its DETOX GREENS product on July 24, 2025, due to potential contamination with pathogenic bacteria. Consumers in 20 states should not consume the product. No injuries have been reported, but the health risk is significant.
Everpress Juice recalled its cashew milk on July 24, 2025, due to under-processing that may lead to pathogenic bacteria contamination. The recall affects consumers in 15 states, posing a high health risk. Consumers should stop using the product immediately and seek a refund or replacement.
Everpress Juice recalled cashew coffee milk on July 24, 2025, due to potential contamination with pathogenic bacteria. The product poses a high risk to consumers' health. Distribution included multiple states across the U.S.
Taizhou Kangping Medical recalled 3.85 million cartons of BZK Antiseptic Towelettes on July 22, 2025. The recall stems from a lack of assurance of sterility, posing a high risk to users. Consumers and healthcare providers must stop using these towelettes immediately.
Middlefield Original Cheese Cooperative recalled 640 pounds of cheese on July 21, 2025. The recall affects Monterey Jack and Farmers Cheese due to potential Listeria monocytogenes contamination. The products were distributed in Kentucky, Ohio, and Pennsylvania.
AUM Pharmaceuticals recalled 50,000 cartons of Quick Touch Alcohol Prep Pads on July 21, 2025, due to cGMP deviations. The recall affects sterile pads containing 70% isopropyl alcohol. Consumers should stop using the product immediately and contact the manufacturer.
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 907 units of the Altivate Reverse Wedge Glenoid Reamer on July 18, 2025, due to a kickback risk during use. The recall affects healthcare providers and patients nationwide across 25 states. This Class II recall warns of potential binding issues that could lead to serious injury.
DJO Surgical recalled 439 AltiVate Reverse Glenoid Trays on July 18, 2025, due to potential reamer malfunction. The reamer may kick or bind during use, posing a serious risk to patients. Healthcare providers should stop using the device immediately and follow the recall instructions.
Quest International recalled 376 Measles IgM Test Kits on July 17, 2025. The kits lack premarket approval or clearance from the FDA. Healthcare providers and patients must stop using these kits immediately.