CPSC•
Louisville Attic Stairway Ladders
Louisville Ladder recalls 1M+ attic stairway ladders over bolt breakage fall hazard.
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CPSC•BUSOHA Magnetic Fidget SlidersBUSOHA recalls 6-pack Magnetic Fidget Sliders due to magnet ingestion hazard; loose magnets can cause serious injury or death.
CPSC•PIXLABBY Magnetic Fidget SlidersPIXLABBY magnetic fidget sliders recalled due to magnet ingestion hazard; can cause serious injury or death.
CPSC•OKK Trading Easter LED HeadbandsOKK Trading recalls Easter LED headbands over accessible coin batteries, posing ingestion hazard.
CPSC•Voomf Play Yard and Crib MattressesVoomf play yard and crib mattresses recalled over entrapment and fire hazards.
CPSC•Syera Projecting Finger Light ToysSyera LED finger lights recalled over accessible button cell batteries that pose ingestion and burn risks.
CPSC•Vanderhall Brawley GTS ROVVanderhall recalls Brawley GTS ROVs (2024-2026) over unintended acceleration crash risk.
CPSC•Courant Spliced Kalimba Climbing RopesCourant recalls Spliced Kalimba climbing ropes due to fall hazard; spliced ends can fail.
CPSC•Winston Porter and Seeday DressersWinston Porter and Seeday dressers recalled due to tip-over and entrapment hazards; violate STURDY Act.
CPSC•Wnttmt Baby WalkersWnttmt baby walkers are recalled for fall and entrapment hazards that violate the infant walker standard.
FDA•MODERATEMirabegron Extended-Release Tablets 25 mgZydus recalls Mirabegron ER 25 mg tablets over nitrosamine impurity.
FDA•MODERATEOribe Serene Scalp Densifying ShampooOribe Serene Scalp Densifying Shampoo recalled over microbial contamination.
FDA•LOWKanni Delight Fresh Frozen Vannamei White ShrimpKanni Delight Fresh Frozen Vannamei White Shrimp recalled over nitrofurans detected in the product.
FDA•MODERATENeuroguard IEP Carotid Stent SystemContego Medical recalls Neuroguard IEP carotid stent system over filter opening failure risk.
FDA•MODERATECOAPTIUM ConnectTISSIUM recalls COAPTIUM Connect nerve repair device over unsubstantiated 36-month shelf life.
8 products
FDA•MODERATEBlom-Singer Classic Indwelling Voice ProsthesisBlom-Singer Classic Voice Prosthesis recalled due to incorrect labeling of flange types.
2 products
FDA•MODERATEGEM Premier 7000 with iQM3Instrumentation Laboratory recalls GEM Premier 7000 with iQM3 due to lysing bag solution concentration issue.
2 products
FDA•MODERATEU2 Total Knee System Femoral Offset BushingU2 Total Knee System femoral offset bushing recalled due to incorrect engraved numbering that may cause misorientation.
2 products
FDA•CRITICALGlutathione 200 mg/mL InjectionVictory Medical Center Pharmacy recalls Glutathione 200 mg/mL vials over bacterial endotoxin contamination.
FDA•MODERATEMedline Hudson RCI Heated Breathing CircuitMedline recalls Hudson RCI heated breathing circuits for infants due to connector thermal damage risk.
5 products
FDA•CRITICALSura Tanmen Hot and Sour Flavor Ramen Noodle KitSura Tanmen ramen noodle kits recalled over undeclared fish in the Soba sauce packet.
FDA•LOWPediatric PN TPN BagsCentral Admixture recalls pediatric TPN bags due to incorrect formulation.
FDA•MODERATERed Blood Cells, Leukocytes ReducedRhode Island Blood Center recalls Red Blood Cells, Leukocytes Reduced units from a malaria-endemic-area donor.
FDA•LOWApheresis PlateletsRed Cross recalls Apheresis Platelets, PAS, Leukocytes Reduced, Pathogen Reduced units lacking required yield testing.
FDA•MODERATEAtellica CH Urine Albumin AssaySiemens recalls Atellica CH Urine Albumin assay over falsely depressed UN_c and A1c_E results and QC failures.
2 products
FDA•MODERATEWangshin Doenjang Soybean PasteWangshin Doenjang soybean paste recalled over undeclared anchovy (fish) allergen.
FDA•MODERATEMicroScan LabPro UpdateBeckman Coulter is recalling MicroScan LabPro Update Panel Update Software Update, MicroScan LabPro Update Panel 11 (US), due to potential incorrect antibiotic resistance results that may lead to delayed or inappropriate treatment.
2 products
FDA•MODERATE5-PLASMA Bivalirudin AMR Verification KitAniara recalls 5-PLASMA Bivalirudin AMR Verification Kit (Model 5D-45905) due to stability issues causing degradation of bivalirudin.
3 products
FDA•MODERATEPhilips Allura Xper Interventional Fluoroscopic X-Ray SystemsPhilips recalls Allura Xper X-ray systems over unauthorized HDDs causing loss of imaging, movement, or data.
5 products
FDA•MODERATEHardyDisk Cefiderocol 30µg Susceptibility DisksHardy Diagnostics recalls HardyDisk Cefiderocol 30µg disks due to incorrect cartridges that may cause false susceptibility results.
FDA•MODERATEU2 Total Knee System PSA Box TrialUnited Orthopedic recalls U2 Total Knee PSA Box Trials (models 9323-5511 thru 9323-5526) due to screw defect.
4 products
FDA•CRITICALBoston Scientific Infinion CX Lead KitBoston Scientific recalls Infinion CX lead kits for SCS systems due to possible lead fracture at anchor site.
FDA•CRITICALBlank Slate Creamery Coconut Fudge SandwichesBlank Slate Creamery recalls Coconut Fudge Sandwiches due to undeclared egg allergen.
FDA•CRITICALKC Everyday Mac & CheeseKerry recalls KC Everyday Mac & Cheese over undeclared egg allergen.
FDA•MODERATEBig Way Hot Pot Miso PasteBig Way Hot Pot Miso Paste recalled for undeclared milk allergen.
FDA•MODERATEDicyclomine Hydrochloride Capsules 10mgAurobindo recalls Dicyclomine HCl 10mg capsules due to shortfill and empty capsules.
FDA•MODERATEGE Portrait Core Services Software V1.2.0GE recalls Portrait Core Services SW V1.2.0 over a security vulnerability.
2 products
FDA•MODERATEHondashi Seasoning PacketsPack'n Fresh recalls Hondashi seasoning packets due to undeclared fish allergen.
FDA•MODERATEFilmArray NGDS Warrior PanelBiofire Defense recalls FilmArray NGDS Warrior Panel due to strain mismatches affecting test accuracy.
FDA•MODERATEGE MAC VU360 ElectrocardiographGE recalls MAC VU360 ECG over software issue that may mix patient data.
FDA•MODERATEMerge PACS Medical Imaging WorkstationMerge PACS workstation recalled over risk of displaying thumbnails from a prior patient study.
2 products
FDA•LOWSyva Emit Tox Tricyclic Antidepressant Calibrator/ControlsSiemens recalls Syva Emit Tox Tricyclic Antidepressant Calibrator/Controls due to out-of-specification sodium azide concentration.
FDA•LOWSyva Emit Disopyramide AssaySiemens recalls Syva Emit Disopyramide Assay due to out-of-spec sodium azide concentration; risk of mild irritation.
FDA•CRITICALbettergoods Pistachio Nut ButterBotticelli Foods recalls bettergoods Pistachio Nut Butter over possible Salmonella contamination.
FDA•MODERATEMaquet Flow Anesthesia Machine VaporizerMaquet recalls Flow anesthesia machines over risk of insufficient anesthesia.
FDA•MODERATEIntramedullary Bone Saw Blade AssemblyBiomet recalls Intramedullary Bone Saw Blade Assembly (Model 475620) over sterile barrier damage risk.
5 products
FDA•MODERATEStryker AHTO Tube Set PackagingStryker recalls AHTO Tube Set Packaging (Cat. 0250070600) over handpiece leaking.
5 products
FDA•MODERATEDialysis Change Tray Clear SequenceMedical Action recalls Dialysis Change Tray Clear Sequence (Model 78791) due to improper seal in needle-free access device.
FDA•MODERATEOXOS MC2 Portable X-Ray SystemOXOS Medical recalls MC2 Portable X-Ray System due to overheating circuit board.
2 products
FDA•MODERATEVector Pedicle Screw System Anti-TorqueInnovasis recalls Vector Pedicle Screw System anti-torque instrument (LS-749) due to undersized tip that may prevent engagement during surgery.