FDA•MODERATE
Maquet Flow Anesthesia Machine Vaporizer
Maquet recalls Flow anesthesia machines over risk of insufficient anesthesia.
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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.
FDA•MODERATEPeter Rabbit Organics Banana & Strawberry PureeCheer Pack recalls Peter Rabbit Organics Banana & Strawberry puree pouches over possible plastic strip release.
FDA•MODERATEAmerican Regent: multiple injectionsAmerican Regent recalls Adequan injections due to particulate matter including glass.
2 products
FDA•CRITICALOptiray 350 Ioversol InjectionLiebel-Flarsheim recalls Optiray 350 Ioversol Injection 500 mL vials due to particulate matter (plastic, steel, glass).
2 products
FDA•Parnell Sevoflurane 250 mLParnell recalls Sevoflurane 250 mL for dogs due to incompatible bottle notch pattern.
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.
FDA•MODERATENerivio Infinity BatteryTheranica recalls Nerivio Infinity over battery thermal-runway risk during charging.
- 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.
- Device RecallFDA•MODERATEREMISOL Advance Data Manager
Beckman Coulter recalls REMISOL Advance Data Manager over software error that may misreport combo assay results.
FDA•CRITICALBD Needle Kit for Powered DriverBard Access recalls BD Powered Driver Needle Kits over obturator removal difficulty.
FDA•MODERATEUkrop's Homestyle Foods: 2 productsUkrop's recalls Bread Pudding with Vanilla Sauce due to possible metal fragments.
2 products
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•Sloosh Dive SticksJoyin expands recall of Sloosh dive sticks over impalement hazard; sticks violate federal ban.
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•TT Trsmima Zipline Kits and Spring BrakesTrsmima recalls zipline kits and spring brakes due to fall and collision hazards from cable detachment and inadequate braking.
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•CRITICALAngiography Procedure Kit ManifoldsAngiography kit manifolds recalled due to particulate risk in blood circulation.
FDA•CRITICALAquafaba Powder529 Commerce recalls Aquafaba Powder over undeclared egg allergen.
FDA•CRITICALPublix Super Markets: Blueberries and Mixed BerriesPublix recalls Organic Whole Blueberries and Mixed Berries over potential E. coli O145:H28 contamination.
4 products
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•MODERATEGalliker Dairy: 2 productsGalliker recalls DQ Chocolate Reduced Fat Ice Cream Mix over possible metal shavings.
2 products
FDA•CRITICALFundamental Feed: 3 Packaged Bopp Woven Plastic WovensFundamental Feed recalls 40 lb forage pellets for horses due to elevated aflatoxin levels.
3 products
FDA•MODERATEEXO Black Tattoo InkXtreme Inks recalls EXO Black tattoo ink due to Pseudomonas aeruginosa contamination.
FDA•MODERATEPhilips Brilliance CT ScannersPhilips recalls Brilliance CT scanners over possible scan trigger failure, risking patient rescan and extra radiation.
3 products