Recalls in Wisconsin (page 8)
4031 recalls.
- ACETABULAR CUP UHMWPE 61-3258 ALL POLY CONSTRAINED INSERT 44MM 69-2244 ... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - DURACON XL ANGLED TIB INS 11/14MM C-M064-1-300 SELF-PRESSURIZING GLENOID SIZE... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - ABG I ACETABULAR INSERT HOODED 28mm ID X 48mm C-M079-2-801 ARC2F ACETABULAR... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - TRIATHLON HINGE INSERT SIZE 4 11MM 5612-P-411 TRIATHLON HINGE INSERT SIZE 4... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - ALL POLY CONSTRAINED INSERT 54MM 69-2854 NRG KNEE CR 82-2-0512 82-2-0518 ... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - OMNIFIT SERIES I ACET. INSERT 10¿ 22mm ID Catalog No. 2001-2246 Orthopaedic... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - AXLE PIN ASSY LARGE ELBOW COBALT CHROME Catalog No. C-M112-2-500 Orthopaedic... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - Captus 4000e Thyroid Uptake System recall (Mirion Technologies (Capintec), Inc.)
Medical deviceClass IIReported September 23, 2026 · Potential for failure of the tension bolt which would allow the spring arm to unexpectedly fall to its lowest position, which is approximately 25 inches (63.5... - Et Control recall (Datex-Ohmeda, Inc.)
Medical deviceClass IIReported September 23, 2026 · Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control... - Aisys CS2 with Et Control recall (Datex-Ohmeda, Inc.)
Medical deviceClass IIReported September 23, 2026 · Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control... - Aisys CS2 recall (Datex-Ohmeda, Inc.)
Medical deviceClass IIReported September 23, 2026 · Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control... - Aisys recall (Datex-Ohmeda, Inc.)
Medical deviceClass IIReported September 23, 2026 · Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control... - Blood Culture Collection Venipuncture Kit 20/Cs recall (Medical Action Industries, Inc. 306)
Medical deviceClass IIReported September 23, 2026 · Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may... - Kinos Axiom Total Ankle System with Axiom PSR recall (restor3d Inc.)
Medical deviceClass IIReported September 23, 2026 · Ankle implantation systems were packaged with incorrect patient-specific cutting guides, which may result in: delayed surgery, the need to use standard... - Brand Name: VERIQA recall (PTW FREIBURG)
Medical deviceClass IIReported September 23, 2026 · When a bolus is included in a treatment plan and sent for secondary dose calculation, the software accounts for it but does not display this clearly, which may... - SunMed Tracheal Tube recall (WELL LEAD MEDICAL CO. LTD)
Medical deviceClass IIReported September 23, 2026 · The 6Fr suction catheter could not pass through the samples smoothly. - Core Services Hub V8 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Workflow Core Services V8 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Centricity PACS Server V7 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Centricity PACS V2 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Enterprise Archive V8 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Centricity Enterprise Archive V2 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - NOxBOXi Nitric Oxide Delivery System. recall (NOXBOX LTD)
Medical deviceClass IIReported September 23, 2026 · Potential for oxygen tubing leaks due to failure of the tubing or tubing connection, which may lead to oxygen desaturation. - Impella Optical Controller recall (Abiomed, Inc.)
Medical deviceClass IReported September 23, 2026 · The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly. - Impella Optical Controller with the below product descriptions and corresponding... recall (Abiomed, Inc.)
Medical deviceClass IReported September 23, 2026 · The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly. - Automated Impella Controller recall (Abiomed, Inc.)
Medical deviceClass IReported September 23, 2026 · The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly. - MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System recall (Bayer Medical Care, Inc.)
Medical deviceClass IIReported September 23, 2026 · Some devices may not have been properly sterilized due to a manufacturing sterilization issue. - Percutaneous Insertion Kit recall (Maquet Cardiopulmonary Gmbh)
Medical deviceClass IIReported September 23, 2026 · The packaging may not consistently maintain sterile barrier integrity. - Percutaneous Insertion Kit recall (Maquet Cardiopulmonary Gmbh)
Medical deviceClass IIReported September 23, 2026 · The packaging may not consistently maintain sterile barrier integrity. - Percutaneous Insertion Kit recall (Maquet Cardiopulmonary Gmbh)
Medical deviceClass IIReported September 23, 2026 · The packaging may not consistently maintain sterile barrier integrity. - Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04 recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported September 23, 2026 · Device may not resume patient monitoring for at least 3 minutes following system restart. Issue can lead to potential delay in recognition of clinically... - Medline Convenience Kit: OPEN HEART A PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · The kits contain a Retrograde Coronary Sinus Perfusion (RCSP) cannulae that has the potential for a sterile barrier breach. Sterility of the product cannot be... - StatStrip Glucose and B- Ketone meter. Model No: 66429. Glucose test system. recall (Nova Biomedical Corporation)
Medical deviceClass IReported September 23, 2026 · A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a... - StatStrip Glucose and B- Ketone meter. Model No: 63910. Glucose test system. recall (Nova Biomedical Corporation)
Medical deviceClass IReported September 23, 2026 · A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a... - StatStrip Glucose and B- Ketone meter. Model No: 63683. Glucose test system. recall (Nova Biomedical Corporation)
Medical deviceClass IReported September 23, 2026 · A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a... - StatStrip Glucose Hospital Meter System. Model No: 66739. Glucose test system. recall (Nova Biomedical Corporation)
Medical deviceClass IReported September 23, 2026 · A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a... - StatStrip Glucose Hospital Meter System. Model No: 63685. Glucose test system. recall (Nova Biomedical Corporation)
Medical deviceClass IReported September 23, 2026 · A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a... - Medline Convenience Kits: 1) DYNDB3086D recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - Medline Convenience Kits: 1) DYNDH1193 recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - Medline Convenience Kits: 1) DYKM1000B recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - Medline Convenience Kits: 1) ACC010308A recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - Medline Convenience Kits: 1) PORT ACCESS KIT UNIV OF ALA recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - Medline Convenience Kits: 1) OPEN HEART ADULT recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - Halyard IV START KIT NON-STERILE REF: KRIV26-02 recall (AVID Medical, Inc.)
Medical deviceClass IReported September 23, 2026 · Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides - Toyworld168 Recalls Rainbow Mystery Squishy Bun Toys Due to Risk of Serious Injury or Death from Water Bead Ingestion; Violate Mandatory Standard for Toys
Consumer productReported September 17, 2026 · The squishy bun toys violate the mandatory safety standard for toys because the water beads inside the dumplings expand larger than permitted, posing a deadly... - Tongyang Cycling Recalls Basecamp Bicycle Helmets Due to Risk of Serious Injury or Death from Head Injury; Violate Mandatory Standard for Bicycle Helmets
Consumer productReported September 17, 2026 · The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, positional... - Sauna360 Recalls Infrared Saunas, Hybrid Infrared Saunas and Infrared Kits Due to Risk of Serious Injury or Death from Fire and Burn Hazards
Consumer productReported September 17, 2026 · The infrared panels in the saunas and kits can short circuit, causing them to overheat, posing a risk of serious injury from fire and burn hazards. - Sauna360 Expands Recall of Tylö Halmstad and Kiruna Hybrid Saunas Due to Fall Hazard; New Remedy Provided
Consumer productReported September 17, 2026 · The saunas contain a bench that can collapse, posing a fall hazard to consumers. The previous recall repair was ineffective; a new repair is now being offered. - SHEIN Distribution Corporation Recalls Pull and Chew Montessori Teething Toys Due to Risk of Serious Injury or Death from Choking Hazard; Violate Mandatory Standard for Toys
Consumer productReported September 17, 2026 · The recalled teething toys violate the mandatory safety standard for toys because the silicone strings are smaller and longer than permitted. The silicone... - Regfear Recalls BedsPick Mattresses Due to Risk of Serious Injury or Death from Fire; Violate Mandatory Flammability Standard for Mattresses
Consumer productReported September 17, 2026 · The mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire. - Melissa & Doug Recalls Fire Truck Activity Board Toys Due to Risk of Serious Injury from Choking Hazard; Sold Exclusively at Target
Consumer productReported September 17, 2026 · The fire hose port can come loose and detach, posing a risk of serious injury from choking hazard. - LANCHEZ Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards
Consumer productReported September 17, 2026 · The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, which may encourage use of an... - JKMAX Recalls Heated Blankets and Heating Pads Due to Fire and Burn Hazards
Consumer productReported September 17, 2026 · The internal wire heating elements of the blankets and pads can overheat, posing fire and burn hazards to consumers. - Hayward Industries Recalls Universal Pool Heaters Due to Risk of Serious Injury or Death from Carbon Monoxide Poisoning Hazard.
Consumer productReported September 17, 2026 · During operation, the heaters can produce high levels of carbon monoxide (CO), posing a risk of serious injury or death from carbon monoxide poisoning. - Friedrich Air Conditioning Recalls KÜHL Window Air Conditioners Due to Risk of Serious Injury or Death from Fire and Burn Hazards
Consumer productReported September 17, 2026 · The control board inside the motor of the recalled air conditioners can fail, posing a risk of serious injury or death from fire and burn hazards. - Esjay US Recalls Toddler Busy Board Montessori Toys Due to Risk of Serious Injury or Death from Choking; Violates Small Parts Ban
Consumer productReported September 17, 2026 · The recalled toy violates the small parts ban because the product is for children under three years of age and the red knobs can detach, posing a deadly... - Colerinsec Recalls Jerify Magnetic Stick Figure Toy Sets Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys
Consumer productReported September 17, 2026 · The magnetic humanoid toy Sets violate the mandatory standard for toys because they can liberate loose high-powered magnets posing an ingestion hazard to... - Char-Broil Recalls Bistro Pro Electric Grills Due to Risk of Electric Shock
Consumer productReported September 17, 2026 · The grounding wire for the grill's heating element can disconnect and lose fault protection, posing an electric shock hazard. - HeartSine SAM 350P 350P US Device recall (HeartSine Technologies Ltd)
Medical deviceClass IIReported September 16, 2026 · Due to a damaged (over stretched) membrane tail that causes an intermittent fault. - Products that contain the Pericare Wipes: recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: SureStep" Foley Tray System Add-A-Foley... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: SureStep Intermittent Catheter Tray REF:... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: *Bardex¿ I.C. Complete Care¿ Foley Catheter... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: Bard¿ Foley Tray With Lubri-Sil¿... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray ... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Prolon Everyday Apulian Almond & Cocoa Spread recall (L-Nutra Inc)
FoodClass IIReported September 16, 2026 · Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio. - 0.9% Sodium Chloride Injection recall (B BRAUN MEDICAL INC)
DrugClass IReported September 16, 2026 · Presence of Particulate Matter: particulate matter identified as iron oxide, inorganic material, cellulose cotton fiber or polystyrene - Epinephrine Injection recall (American Regent, Inc.)
DrugClass IReported September 16, 2026 · Presence of Particulate Matter and Lack of Assurance of Sterility. Particulate matter identified as nylon, cellulosic, acrylic, polyethylene and glass and... - fentaNYL Citrate recall (OurPharma LLC)
DrugClass IIReported September 16, 2026 · Labeling: Not Elsewhere Classified: Complaint received on 08/31/2026 regarding the discrepancy of the IV bag expiry (07/31/2026 and 11/30/2026) and the product... - Dextrose Injection recall (Baxter Healthcare Corporation)
DrugClass IReported September 16, 2026 · Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution. - Fluphenazine Hydrochloride Tablets recall (Ajanta Pharma USA Inc)
DrugClass IIIReported September 16, 2026 · Failed impurities/degradation specifications: (OOS) for Organic Impurities by HPLC (Impurity-A) during testing at the 18 months long term stability. Result... - Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution recall (ImprimisRx NJ LLC)
DrugClass IIIReported September 16, 2026 · Subpotent Drug - AMS Convenience Kit: DSAEK Pack - RX recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported September 16, 2026 · The convenience kits contain .0.9% Sodium Chloride Injection, USP products in Single Dose freeflex bags, which may contain blue Break-off-Parts (BOPs) that... - Citric Complete Liquid Citric Acid Concentrate REF: LC+200-D recall (Nipro Renal Soultions USA, Corporation)
Medical deviceClass IIReported September 16, 2026 · Hemodialysis concentrates contain high endotoxin levels - Citric Complete Dry Citric Acid Concentrate REF: DCA+200-25 & DCA+203-25 recall (Nipro Renal Soultions USA, Corporation)
Medical deviceClass IIReported September 16, 2026 · Hemodialysis concentrates contain high endotoxin levels - MedicaLyte Bicarbonate Powder REF: DB+201-2.1 recall (Nipro Renal Soultions USA, Corporation)
Medical deviceClass IIReported September 16, 2026 · Hemodialysis concentrates contain high endotoxin levels - MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201 recall (Nipro Renal Soultions USA, Corporation)
Medical deviceClass IIReported September 16, 2026 · Hemodialysis concentrates contain high endotoxin levels - Getinge PVC Thoracic Catheter recall (Atrium Medical Corporation)
Medical deviceClass IIReported September 16, 2026 · An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. - Getinge PVC Thoracic Catheter recall (Atrium Medical Corporation)
Medical deviceClass IIReported September 16, 2026 · An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. - Getinge PVC Thoracic Catheter recall (Atrium Medical Corporation)
Medical deviceClass IIReported September 16, 2026 · An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. - Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser... recall (Lutronic Corporation)
Medical deviceClass IIReported September 16, 2026 · Utilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment, potentially resulting in... - Halyard IV Start Kit Non-Sterile REF: KRIV26-02 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 16, 2026 · Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper... - Bravo CF capsule delivery device recall (Given Imaging Ltd.)
Medical deviceClass IReported September 16, 2026 · Capsule may fail to attach to the esophagus or detach from the delivery device. Risks include patient aspiration/inhalation, perforation of esophagus... - ZMC Group Expands Recall of Light-Up Children’s Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
Consumer productReported September 10, 2026 · The recalled light-up toys violate the mandatory safety standard for children’s toys because the toys contain button cell batteries that can be easily accessed... - FJTJBSI Recalls Six-Drawer Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units
Consumer productReported September 10, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - Triumph Motorcycles Recalls Closed Course Competition Motorcycles Due to Risk of Serious Injury or Death from Crash Hazard
Consumer productReported September 10, 2026 · The engine rocker arm on the recalled motorcycles can seize or stick and the exhaust valves can remain open or break, posing a risk of serious injury or death... - Cade California Electronic Recalls Finger Light Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
Consumer productReported September 10, 2026 · The recalled finger lights violate the mandatory safety standard for toys because the toys contain button cell batteries that can be easily accessed by... - Dual Fuel Ranges Recalled Due to Risk of Serious Injury or Death from Fire or Explosion Hazards; Manufactured by AGA Rangemaster
Consumer productReported September 10, 2026 · Dual Fuel Ranges with a missing cap from the gas test port can cause a gas leak, posing a risk of serious injury or death from fire or explosion hazards. - Prepared Hero Recalls Fire Spray Canisters Due to Risk of Serious Injury or Death from Fire and Burn Hazards
Consumer productReported September 10, 2026 · The recalled fire spray canister can deteriorate overtime, causing it to rupture and fail to operate during a fire, posing the risk of serious injury or death... - Guang Zhou Recalls Wantefully Hair Dryer Brushes Due to Risk of Serious Injury or Death from Electrocution, Shock and Burn Hazards; Violate Federal Regulations
Consumer productReported September 10, 2026 · The recalled hair dryer brushes are in violation of federal regulations for hair dryers as they lack an integrated immersion protection device, which presents... - SQT Recalls Lontcs Busy Boards Due to Risk of Serious Injury from Lead Poisoning; Violate Federal Lead Paint Ban
Consumer productReported September 10, 2026 · The toys’ zipper contains levels of lead that exceed the standard set in the federal lead paint ban. Lead is toxic if ingested by young children and can cause... - Sweet Cubby Recalls Children's Loungewear Sets Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Children's Sleepwear
Consumer productReported September 10, 2026 · The recalled children’s loungewear sets violate the mandatory flammability standard for children’s sleepwear, posing a risk of serious burn injuries or death. - Junkins Recalls DHASUWT Hair Dryer Brushes Due to Risk of Serious Injury or Death from Electrocution, and Shock Hazards; Violate Federal Regulations; Smoking and Fire Hazards
Consumer productReported September 10, 2026 · The recalled hair dryer brushes lack an integrated immersion protection device, which presents a substantial product hazard to consumers, posing the risk of... - Victgoal Recalls Bicycle Helmets Due to Risk of Serious Injury or Death from Head Injury; Violate Mandatory Standard for Bicycle Helmets
Consumer productReported September 10, 2026 · The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the retention system, positional... - Ricky Joy Recalls More Than 2.3 Million Sour Crush Candy Bottles Due to Risk of Serious Injury or Death from Choking Hazard
Consumer productReported September 10, 2026 · The rolling ball on the recalled candy bottles can detach, posing a risk of serious injury or death from choking hazard. - Baxter Novum IQ Syringe Pump recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 9, 2026 · A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused... - Baxter Novum IQ Syringe Pump recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 9, 2026 · A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused... - HEALON EndoCoat PRO recall (Johnson & Johnson Surgical Vision, Inc.)
Medical deviceClass IIReported September 9, 2026 · Surgical instructions sent for viscoelastic products used during ophthalmic viscosurgical cataract procedures including in part: If resistance is encountered... - THE HAMPTON GROCER brand recall (THE HAMPTON GROCER)
FoodClass IReported September 9, 2026 · Product may be contaminated with Salmonella.