CPSC•
Kmaier Infant Walkers
Kmaier infant walkers violate the federal safety standard, posing a fall hazard that can cause serious injury or death.
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Back to home ←- CPSC•Kmaier Infant Walkers
Kmaier infant walkers violate the federal safety standard, posing a fall hazard that can cause serious injury or death.
- CPSC•Kmaier Infant Walkers
Kmaier infant walkers violate the federal safety standard, posing a fall hazard that can cause serious injury or death.
CPSC•Little Loves & Co. Youth Clothing with DrawstringsLittle Loves & Co. recalls youth clothing with waist drawstrings over entrapment hazard.
- CPSC•Kmaier Infant Walkers
Kmaier recalls infant walkers over fall hazard; they violate federal safety standard.
CPSC•YERYORK Pressure WashersYERYORK pressure washers, model YE-006, recalled over missing GFCI posing shock and electrocution hazards.
CPSC•Steelite Pressure WashersSteelite pressure washers, model AZ6041VC, recalled over shock and electrocution hazards from missing GFCI.
CPSC•Chillife Montessori Baby Toy SetsChillife Montessori Baby Toy Sets recalled due to choking hazard from pull string teether.
CPSC•Mainstays Nine-Drawer Fabric DressersWalmart reannounces recall of Mainstays nine-drawer fabric dressers over tip-over and entrapment hazards.
FDA•Feline Milk ReplacerRevival Animal Health recalls feline milk replacers over low nutrient levels.
FDA•MODERATERamipril Capsules USP 10 mgHikma recalls Ramipril Capsules USP 10 mg over a failed impurity (DCU) specification.
FDA•MODERATEICU Medical IV Sets with Drip ChambersICU Medical recalls IV sets with drip chambers due to black specks that may delay therapy.
FDA•LOWAfricando Alfredo Hot SauceAfricando Alfredo Hot Sauce recalled for undeclared wheat and soy allergens.
FDA•MODERATEByron White Formulas: 3 May Contain Nuts CasByron White Formulas recalls A-L Complex, A-FNG, and A-P herbal supplements due to undeclared walnuts.
3 products
FDA•MODERATEOlympus PowerSeal 5 mm Curved Jaw Sealer & DividerOlympus recalls PowerSeal 5 mm Curved Jaw Sealer & Divider over labeling error.
FDA•MODERATEZicam Medicated Nasal SwabsZicam nasal swabs recalled over microbiological testing failures.
FDA•MODERATEIMRIS ORT200 Operating Room TableIMRIS recalls ORT200 operating room tables due to actuator/lock failure risk of unintended movement.
2 products
FDA•MODERATEActhar Gel (Repository Corticotropin Injection) 5 mL VialsMallinckrodt recalls Acthar Gel 5 mL vials over glass and stopper particulate.
2 products
FDA•MODERATEClobetasol Propionate Cream USP, 0.05%Lupin recalls Clobetasol Propionate Cream 0.05% due to failed content uniformity.
FDA•MODERATEhealthmark ProChek-II TestHealthmark recalls ProChek-II tests (PT-313, PT-201-12) over expired ingredient risk.
2 products- Device RecallFDA•MODERATEFUJIFILM Synapse PACS Software
FUJIFILM Synapse PACS v7.4.310 recalled due to inaccurate ruler measurements.
FDA•MODERATEMedline Femoral Pack and FEVAR KitsMedline recalls Femoral Pack and FEVAR kits due to potentially contaminated component.
14 products
FDA•MODERATEGENESYS CrossFT Suture AnchorConMed recalls GENESYS CrossFT Suture Anchor (REF CFBC-5502B) due to incorrect implant card.
FDA•MODERATEFresenius 2008T BlueStar Hemodialysis MachineFresenius recalls 2008T BlueStar Hemodialysis Machine over flow, no water, and temperature alarms.
FDA•CRITICALBaxter Dextrose Injection 70% 2000 mL BagsBaxter recalls Dextrose Injection 70% 2000 mL bags over stainless steel particles.
FDA•Baxter 0.9% Sodium Chloride Injection 500 mLBaxter recalls 0.9% Sodium Chloride Injection 500 mL VIAFLEX bags over fiberglass particulate contamination.
FDA•CRITICALJalapeno RanchJaime's Foods recalls Jalapeno Ranch 16 oz jars due to undeclared egg allergen.
FDA•Baxter Anticoagulant Sodium Citrate SolutionBaxter International is recalling one lot of Anticoagulant Sodium Citrate Solution for potential presence of particulate matter (fiberglass).
FDA•LOWIbuprofen Oral Suspension SyringesSafecor recalls Ibuprofen oral suspension syringes over cross-contamination risk.
FDA•MODERATEStructur 2 SC Temporary Resin Cartridge RefillHenry Schein recalls Structur 2 SC Temporary Resin Cartridge Refill 75Gm due to incorrect packaging and IFU.
2 products
FDA•MODERATEMidmark IQecg Digital ECGMidmark recalls IQecg Digital ECG over incorrect ECG waveforms and BPM calculations.
2 products
FDA•MODERATECanon Alphenix Ceiling Movement Gear ScrewsCanon recalls Alphenix X-ray systems (INFX-8000C/F/V) over loose ceiling gear screws.
FDA•Vitruvias Thyroid Tablets 30 mgVitruvias recalls one lot of Thyroid Tablets 30 mg over potential super potency.
FDA•Momchipz Veggie Chips Broccoli Florets & CauliflowerMomchipz Veggie Chips recalled due to undeclared wheat; sold on Amazon.
FDA•Donutful Chocolate Dipped Vanilla Cake DonutsDonutful Chocolate Dipped Vanilla Cake Donuts recalled due to undeclared milk allergen.
FDA•CRITICALTyenne (tocilizumab-aazg) Injection 400 mg/20 mLFresenius Kabi recalls Tyenne ( (tocilizumab-aazg) 400 mg/20 mL vials over glass particles.
FDA•MODERATERemedy+ Recovery Dogswell Pet WormerRemedy+ Recovery Dogswell Pet Wormer recalled due to adverse event complaints.
FDA•Everything Sprouts Alfalfa SproutsEverything Sprouts recalls Alfalfa Sprouts over potential E. coli and Salmonella contamination.
FDA•CRITICALFromm Family Foods: 2 Wet Dog Food Packaged In CodesFromm recalls Turkey Pate and Milo's Meatloaf Pate wet dog foods over possible metal contamination.
2 products
FDA•CRITICALSirna & Sons Jalapeño Peppers 1 lbSirna & Sons recalls 1 lb jalapeño peppers over potential Salmonella Javiana.
FDA•MODERATELevothyroxine Sodium Tablets 25 mcgAccord recalls Levothyroxine 25 mcg tablets due to subpotency.
12 products
FDA•MODERATEHalyard Davinci TruCustom Foley TrayHalyard Davinci TruCustom Foley tray recalled over missing latex warning on StatLock component.
8 products
FDA•MODERATEMerge PACS and Merge OrthoPACSMerge PACS and OrthoPACS recalled due to inaccurate measurement display.
FDA•MODERATEAmerican Contract System Convenience KitAmerican Contract Systems recalls Convenience Kit CV B PACK (TNCB10AM) due to catheter performance failure.
4 products- Device RecallFDA•MODERATEPhilips Incisive CT Software
Philips Incisive CT software V4.5/V5.0 recalled for Bolus Tracking scan trigger failure.
FDA•MODERATEMedline Trach Tube KitMedline recalls Trach Tube Kit (SKU DYKM2330) over labeling discrepancy.
FDA•MODERATEOnli Hydrophilic Urethral Intermittent CathetersHollister recalls Onli intermittent catheters due to a protrusion defect that may cause genitourinary trauma or bleeding.
2 products
FDA•MODERATEMedline ENT Convenience KitsMedline recalls ENT/sinus kits with Pilling Wecksorb Neurosponges over endotoxin risk.
6 products
FDA•MODERATEDouble Golden Fish Galanga PowderTang's Family recalls Double Golden Fish Galanga Powder due to elevated lead levels.
CPSC•CCM FMHVR Hybrid Visors and ACCHVR Replacement Visor AccessoriesCCM recalls FMHVR Hybrid Visors and ACCHVR Replacement Visor Accessories due to risk of laceration or impact injury from cracking.