FDA•MODERATE
U2 Total Knee System PSA Box Trial
United Orthopedic recalls U2 Total Knee PSA Box Trials (models 9323-5511 thru 9323-5526) due to screw defect.
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FDA•CRITICALKC Everyday Mac & CheeseKerry recalls KC Everyday Mac & Cheese over undeclared egg 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•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•MODERATEMaquet Flow Anesthesia Machine VaporizerMaquet recalls Flow anesthesia machines over risk of insufficient anesthesia.
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.
FDA•CRITICALOptiray 350 Ioversol InjectionLiebel-Flarsheim recalls Optiray 350 Ioversol Injection 500 mL vials due to particulate matter (plastic, steel, glass).
2 products
FDA•CRITICALHalyard Cardiac Cath Pack with Medline ManifoldAVID Medical recalls Halyard kits with Medline manifolds due to particulate risk.
3 products
FDA•MODERATEmunevo DRIVE Powered Wheelchair Control SystemMunevo recalls wheelchair control systems over software calibration issue causing steering drift and collision risk.
- Device RecallFDA•MODERATEWASPLab WebApp Software
Copan WASP recalls WASPLab WebApp software over a result-overwrite issue.
FDA•MODERATERadial Jaw 4 Biopsy ForcepsBoston Scientific recalls Radial Jaw 4 biopsy forceps due to sterile barrier breach risk.
4 products
FDA•MODERATEFORWARD Oral Airway KitIntegrated Medcraft recalls FORWARD Oral Airway Kits due to possible occluded airway tip.
2 products- Device RecallFDA•MODERATEQuantum 4Front 2 Wheelchair Controller
Quantum Rehab recalls the Quantum 4Front 2 wheelchair controller over a software issue that can cause unexpected park brake stops.
13 products 
FDA•MODERATETherabody Theragun G4 PRO ChargerTherabody recalls Theragun G4 PRO charger due to fire risk from overheating cradle.
FDA•CRITICALBD Needle Kit for Powered DriverBard Access recalls BD Powered Driver Needle Kits over obturator removal difficulty.
CPSC•EnHomee 15-Drawer DressersEnHomee 15-Drawer Dressers recalled for tip-over and entrapment hazards; violate STURDY Act.
CPSC•KAIFAM 5-Drawer DressersKAIFAM 5-Drawer Dressers recalled for tip-over and entrapment hazards; violate STURDY Act safety standards.
CPSC•BenQ GV31 Portable ProjectorsBenQ recalls GV31 portable projectors due to lithium-ion battery overheating fire and burn hazard.
CPSC•Galanz Retro RefrigeratorsGalanz recalls retro refrigerators due to fire risk; one death reported. Models BCD-215V-62H, GLR76TRDER, GLR76TBKER, GLR76TBEER, GLR76TWEER affected.
CPSC•Fantastic Four Cups and Captain America Popcorn Helmet ContainersGolden Link recalls Fantastic Four cups and Captain America popcorn helmet containers with LED lights over accessible button cell batteries posing ingestion hazard.
CPSC•Nordi Toddler Tower StoolsHARPPA recalls Nordi toddler tower stools over collapse, tip-over, and entrapment hazards.
CPSC•OCTROT Heated Sherpa Throws and BlanketsOCTROT heated throws and blankets recalled due to fire and burn hazards from detachable cord. Models OCT-5060, OCT-5062, OCT-6248, OCT-7284, OCT-8490.
CPSC•World Class Fireworks Skull Strobe RocketsJake's Fireworks recalls Skull Strobe rockets due to premature explosion and burn hazards.
CPSC•Mangohood Direct Kids Kitchen Standing TowersMangohood Direct children's tower stools, model LT003, pose tip-over, fall, and entrapment hazards.
CPSC•Mommy's Baby Lovely Deluxe Baby Doll PlaysetTOYHW recalls Mommy's Baby Lovely Deluxe Baby Doll Playset, model NEW319A, due to small parts choking hazard.
CPSC•OCOOPA Rechargeable Hand WarmersOCOOPA recalls 1.5M rechargeable hand warmers over fire and burn risk; one death reported.
CPSC•Cpzzkq Baby LoungersCetoPMax expands Cpzzkq baby lounger recall over suffocation hazard; 195 more loungers in green and purple added.
CPSC•Woodure Toddler Kitchen Step StoolsWoodure toddler step stools (models WD1764, WD1357, WD1720) pose entrapment and fall hazards that can cause serious injury or death.
FDA•MODERATEPower Over Fiber Base ModuleTerex Utilities recalls Power Over Fiber Base Module due to missing laser certification and improper labeling.
FDA•CRITICALAquafaba Powder529 Commerce recalls Aquafaba Powder over undeclared egg allergen.
FDA•MODERATEStryker Hoffmann II Connecting Rod Micro 3 x 30mmStryker recalls Hoffmann II Connecting Rod Micro 3 x 30mm due to potential cracking after cleaning and sterilization.
7 products
FDA•MODERATEGEM Premier 5000/7000 Bar Code Reader WandInstrumentation Laboratory recalls BCR Wand for GEM Premier 5000/7000 analyzers; may assign results to wrong patient ID.
10 products
FDA•MODERATEAzelaic Acid Gel 15%Glenmark recalls Azelaic Acid Gel 15% over grainy/gritty texture complaints.
FDA•MODERATEMellish Island Super Skin Dietary SupplementMellish Island Super Skin supplement recalled for undeclared fish allergen in marine collagen.
FDA•MODERATEOsteoBallast 45 x 17.5 mmIsoTis recalls OsteoBallast 45 x 17.5 mm DBM mesh due to underfill, risking incomplete fusion.
FDA•CRITICALResmed Astral 100/150 VentilatorResMed recalls Astral 100/150 ventilators due to supercapacitor leakage that may interrupt ventilation.
FDA•MODERATEPhilips Brilliance CT ScannersPhilips recalls Brilliance CT scanners over possible scan trigger failure, risking patient rescan and extra radiation.
3 products
FDA•MODERATEAMS Spinal KitAMS SPINAL KIT recalled due to supplier quality issues with included Lidocaine HCl injection.
9 products
FDA•MODERATEMedtronic EOPA Arterial Cannula 22FRMedtronic recalls EOPA 22FR arterial cannula (Model 77422) over pinhole leak risk during bypass.
6 products
FDA•CRITICALRelax 5-HTP Plus Vitamin B6Relax 5-HTP Plus Vitamin B6 recalled for elevated 5-HTP levels above allowed dosage.
2 products
FDA•CRITICALCefazolin in Dextrose InjectionBaxter recalls Cefazolin in Dextrose 2g/100mL infusion bags due to particulate matter.
FDA•CRITICALAmerican Regent: Multiple Packaged In InjectionsAmerican Regent recalls Nitroglycerin Injection 50 mg/10 mL and other injectables due to particulate matter (hair).
14 products