1278 alerts recorded, refreshed every six hours. Filter by source or category.
Tiffany Food Corp's Hexing Haw Balls candy, packaged in 200g clear plastic bags, is affected. The candy contains unapproved dye Ponceau 4R, posing a risk to consumers who purchased it. Consumers should not eat the candy and should return or discard it.
NatureBest Pre-Cut & Produce LLC recalled its Pico de Gallo Hot (6/9oz) and HEB Pico de Gallo Hot (12/14oz) products. The jalapenos in these items may be contaminated with Salmonella, posing a risk to consumers in Texas and Louisiana. Consumers should not eat these products and should return or discard them.
Taylor Fresh Foods Inc is recalling its Tomato Salsa Fresca in 4-pound containers. The salsa may be contaminated with Salmonella, posing a risk to consumers in many U.S. states. Consumers should not eat it and should discard or return it for a refund.
Everything Sprouts, LLC is recalling its Everything Sprouts Crunchy Protein Sprout Mix in 5.0 oz packages sold in Minnesota and Wisconsin. The sprouts may be contaminated with STEC E. coli and Salmonella, which can cause serious illness in consumers. Consumers should not eat the product and should return or discard it.
Toyworld168 recalls Rainbow Mystery Squishy Bun Toys, translucent green squishy toys with glitter and water beads in a tan plastic container. The water beads expand beyond the allowed size, posing ingestion, choking, and intestinal obstruction hazards that can cause severe illness or death to children. Consumers must immediately stop using the recalled toys and keep them away from children.
Basecamp bicycle helmets, model HT-10, are recalled by Tongyang Cycling. The helmets violate the mandatory bicycle helmet standard and pose a risk of serious head injury or death to wearers. Consumers should stop using the recalled helmets.
The recall affects Basecamp-branded bicycle helmets, model HT-10, sold in green and black in size M/L. Users face risk of serious head injury or death because the helmets fail mandatory safety standards, and the button cell battery can cause internal burns if swallowed. Consumers should stop using these helmets immediately.
SHEIN Distribution Corporation recalled its Pull and Chew Montessori Teething Toys. The silicone strings are smaller and longer than allowed, can lodge in the throat, and pose a deadly choking hazard to infants and young children. Consumers should stop using the recalled teething toys and keep them away from children.
SHEIN Distribution Corporation recalled its Pull and Chew Montessori Teething Toys. The silicone toys pose a choking hazard that can cause serious injury or death to young children. Consumers should stop using the recalled toys immediately.
Sauna360 is recalling its infrared saunas, hybrid infrared saunas, and infrared kits. The infrared panels can short circuit and overheat, posing fire and burn hazards to users. Consumers should stop using the recalled products and contact Sauna360 to determine if their unit is included.
Sauna360 is recalling Tylö Halmstad and Kiruna Hybrid sauna rooms. The bench can collapse, posing a fall hazard to consumers, and the earlier repair was ineffective. Consumers should stop using the sauna and contact Sauna360 for the new repair.
Regfear is recalling BedsPick brand mattresses, 12-inch queen size with white tops and purple or gray sides, sold compressed in a box. The mattresses violate the mandatory flammability standard, posing a risk of serious injury or death from fire to consumers. Consumers should check the sewn-in white label for prototype IDs AMGSW066 or AMGSW067 and model numbers SME004 or AMG005197_12_Q_GLT.
Melissa & Doug recalls its Lights and Sound Fire Truck Activity Board toy, sold exclusively at Target. The fire hose port can come loose and detach, posing a serious choking hazard to young children. Consumers should stop using the recalled toy and contact Melissa & Doug or Target for a refund or replacement.
Melissa & Doug is recalling its Lights and Sound Fire Truck activity board toy, sold exclusively at Target. The black plastic fire hose connector can detach, posing a choking hazard to young children. Consumers should stop using the toy and return it to Target or contact Melissa & Doug for a refund.
The recall involves LANCHEZ-branded electric pressure washers, model KLC-BULL135C, sold in blue-and-black or red-and-black. The units lack a ground-fault circuit-interrupter and adequate power cord, which can cause use of extension cords and expose users to serious shock or electrocution hazards. Consumers must stop using the recalled pressure washers immediately and contact LANCHEZ for a refund or replacement.
JKMAX heated blankets and heating pads are recalled. The internal wire heating elements can overheat, posing fire and burn hazards to consumers. Consumers should stop using the recalled products and contact JKMAX for a refund or replacement.
Hayward Industries recalls its HDFS400 Universal-HC Series pool heaters, 400,000 BTU dual-fuel gas units. The heaters can emit high levels of carbon monoxide during operation, posing a risk of serious injury or death to users. Consumers should immediately stop using the recalled heaters and contact Hayward for a free repair or replacement.
Friedrich Air Conditioning is recalling KÜHL Q and KÜHL S window air conditioners. The motor's control board can fail, posing fire and burn hazards that can cause serious injury or death to consumers. Consumers should find the model and serial number inside the unit and contact Friedrich to see if their air conditioner is included.
The recalled product is the Esjay Toddler Busy Board Montessori Toys, a blue felt board with cartoon dinosaurs and alphabet squares. The red knobs can detach, posing a deadly choking hazard to children under three years old. Consumers should stop using the toy and contact Esjay US for instructions.
The recall affects Jerify Magnetic Humanoid Toy Sets 30 PCS, magnetic stick figure toys. The toys can release loose high-powered magnets, which if swallowed by children can cause intestinal perforation, blockage, blood poisoning, and death. Consumers must stop using the recalled toys immediately and keep them away from children.
The recall affects Char-Broil Bistro Pro Electric Grills with date codes 2510, 2511, or 2512. The grounding wire can disconnect, causing an electric shock hazard to users. Consumers should check the date code on the label to see if their grill is included.
B. Braun Medical Inc. is recalling its 0.9% Sodium Chloride Injection, USP, 100 mL Partial Fill in 150 mL PAB Container. The sterile IV solution may contain particulate matter such as iron oxide, cellulose, or polystyrene, posing a risk to patients receiving it. Consumers should stop using the product and return it or contact B. Braun for instructions.
American Regent, Inc. is recalling Epinephrine Injection, USP, 30 mg/30 mL (1mg/mL), 30 mL multiple-dose vials. The vials may contain particulate matter such as nylon, glass, and other materials, and may be broken or leaking, posing a risk of contamination and lack of sterility to patients receiving the injection. Consumers should stop using the recalled vials and return them to their pharmacy or contact their healthcare provider for guidance.
OurPharma LLC is recalling fentaNYL Citrate injection solution in 100 mL bags. The hazard is a labeling discrepancy between the IV bag expiry and the product expiry, exposing patients to potentially expired medication. Consumers should stop using the affected product and return it to the pharmacy or contact OurPharma LLC.
Getinge PVC Thoracic Catheters, Soft PVC Right Angle, in sizes 24FR, 28FR, 32FR, and 36FR, are recalled. The catheters may contain elevated bacterial endotoxins, posing a risk of fever or severe reaction to patients. Consumers should stop using the recalled catheters and contact Getinge/Atrium Medical for return and replacement instructions.
C.R. Bard Inc. is recalling certain Bardex and SureStep Foley Catheter Trays that contain Pericare Wipes. The wipes may be contaminated on their surface, posing a risk to patients using these urological catheter trays. Consumers should stop using affected products and contact C.R. Bard or the FDA for instructions.
The recall affects Given Imaging Ltd. Bravo CF capsule delivery devices, product numbers FGS-0635 and FGS-0636, used to attach a pH monitoring capsule to the esophagus. The capsule may fail to attach or detach, exposing patients to aspiration, esophageal perforation, airway obstruction, bleeding, laceration, delayed diagnosis, or retained foreign bodies. Consumers should stop using the affected devices and contact their healthcare provider.
Nipro Renal Solutions USA Corporation is recalling Citric Complete Dry Citric Acid Concentrate, references DCA+200-25 and DCA+203-25. The concentrate has high endotoxin levels, which can cause fever or severe reactions in hemodialysis patients. Consumers should stop using the recalled product and contact their dialysis provider or Nipro for instructions.
C.R. Bard Inc. is recalling Pericare Wipes included in SureStep Intermittent Catheter Trays and Preamendment trays. The wipes may have surface contamination, exposing patients using these urological catheter trays to potential infection. Consumers should stop using the affected trays and contact C.R. Bard for instructions.
The recall affects Medical Action Industries' Epidural/Pain TQC kit, REF 82465, containing Sodium Chloride Injection 0.9% USP 10ml ampules. The hazard is potentially compromised sterility, exposing patients who receive these kits to infection risk. Consumers should stop using the recalled kits and contact the firm for return or replacement.
AVID Medical, Inc. is recalling the Halyard IV Start Kit Non-Sterile REF: KRIV26-02. The kits contain applicators that lack sterility assurance due to wrinkles in the paper lidding, exposing patients to infection risk. Consumers should stop using the affected kits and follow the recall instructions.
Medical Action Industries is recalling its Single Shot Epidural kits, references 59553 and 83945B, which contain 0.9% sodium chloride injection ampules. The kits may have compromised sterility, posing a risk to patients receiving epidural procedures. Consumers should stop using the recalled kits and contact Medical Action Industries for instructions.
Windstone Medical Packaging, Inc. is recalling its AMS Convenience Kit: DSAEK Pack - RX, Part Number AMS12394B. The kits may contain blue Break-off-Parts that detached from the infusion port, posing a hazard to patients. The firm initiated a voluntary recall of the affected kits.
Nipro Renal Solutions USA Corporation is recalling MedicaLyte Bicarbonate Powder in specific REFs. The powder contains high endotoxin levels, posing a risk to hemodialysis patients. Consumers should stop using the recalled powder and follow the firm's recall instructions.
C.R. Bard Inc. is recalling SureStep Foley Tray Systems and Bardex IC Complete Care products that contain Pericare Wipes. The wipes may have surface contamination, exposing patients using these urological catheter trays to potential infection. Consumers should stop using the affected products and follow the firm's recall instructions.
Nipro Renal Solutions USA is recalling Citric Complete Liquid Citric Acid Concentrate in refs LC+200-D, LC+201, and LC+225(45X). The concentrate contains high endotoxin levels, posing a risk to hemodialysis patients. Consumers should stop using the recalled product and follow the company's recall instructions.
Getinge PVC Thoracic Catheters, firm PVC straight, in sizes 28FR and 36FR, are affected. The catheters may contain bacterial endotoxin, posing a risk of infection or reaction to patients. Consumers should stop using the affected catheters and contact Getinge or their healthcare provider for instructions.
C.R. Bard is recalling certain Foley and intermittent catheter trays that include Pericare Wipes. The wipes may be contaminated on their surface, posing a risk to patients who use these urological devices. Consumers should stop using affected trays and follow the recall instructions for return or replacement.
The recall affects HeartSine Technologies' SAM 350P, 360P, and 450P defibrillators sold worldwide including the U.S. A damaged membrane tail can cause intermittent faults, exposing cardiac arrest patients to device failure. Consumers should contact HeartSine Technologies for instructions on returning or repairing affected devices.
C.R. Bard Inc is recalling products containing Pericare Wipes, including Bard Foley Tray with Lubri-Sil All-Silicone Foley Catheter and other catheter tray systems. The wipes have surface contamination, exposing patients using these catheter trays to potential infection. Consumers should consult the FDA recall notice for instructions on affected products.
Getinge PVC Thoracic Catheter, Soft PVC Straight, in sizes 16FR to 36FR, is affected. The hazard is an out-of-specification bacterial endotoxin test result in a single lot, exposing patients nationwide. Consumers should be aware that the recall is voluntary and firm-initiated.
C.R. Bard Inc. is recalling SureStep Foley Tray Systems and SureStep Intermittent Catheter Tray that contain Pericare Wipes. The wipes may have surface contamination, exposing patients to possible infection during urological use. Consumers should stop using affected products and contact C.R. Bard for return instructions.
The Lutronic DermaV Laser System is affected. Using higher fluences at 1064nm with current cryogen settings can cause a spark or loud noise, potentially burning patients. Consumers should contact Lutronic Corporation for recall instructions.
Nipro Renal Solutions USA Corporation is recalling MedicaLyte Liquid Bicarbonate Concentrate REF BC-100 and BC+201. The concentrate has high endotoxin levels, posing a risk to hemodialysis patients. Consumers should stop using the recalled product and follow the firm's recall instructions.
Baxter Healthcare Corporation is recalling Dextrose Injection, USP, 70%, 2000 mL bags, a prescription drug. The solution contains stainless steel particles, posing a hazard to patients who receive the injection. Consumers should stop using the affected product and contact their healthcare provider.
Ajanta Pharma USA Inc. is recalling Fluphenazine Hydrochloride Tablets, USP, 1mg, 100-count bottles. The tablets failed impurity specifications, exposing patients to a slightly higher level of impurity-A. Consumers should check their bottles and contact their pharmacist or doctor for instructions.
ImprimisRx NJ LLC is recalling Povidone Iodine 1.25% and Proparacaine HCl 0.5% Ophthalmic Solution, 10 mL dropper bottles, distributed nationwide. The product is subpotent, meaning it may not work as intended, exposing patients to inadequate disinfection or anesthesia during eye procedures. Consumers should stop using the recalled solution and return it to the place of purchase or contact the company for a refund.
Ferrero USA is recalling Fannie May & XO Marshmallow Pixie S'mores Collection, 4.47oz. The product contains undeclared milk and pecans, which can cause serious reactions in people with allergies, and was sold in Iowa, Illinois, Indiana, and Ohio. Consumers who bought this product should not eat it and should return or discard it according to the recall notice.
International Specialty Supply alfalfa in 50-pound bags is recalled. The product may contain E. coli and Salmonella, posing a risk to anyone who eats it. Consumers should not eat the recalled alfalfa and should return it to the place of purchase.
Exotique Foods Canada is recalling Momchipz Gluten Free Veggie Chips Broccoli Florets & Cauliflower in 3oz packages with UPC 6 28634 44216 6. The chips contain undeclared wheat, posing a risk to people with a wheat allergy or celiac disease. Consumers who bought them should not eat the product and should return or discard it.
Data comes from official CPSC and FDA publications (United States). Summaries are generated automatically from those publications: the cited source prevails.