CPSC•
Thermos Stainless King Food Jars and Bottles
Thermos is recalling 8.2M Stainless King Food Jars (SK3000, SK3020) and Sportsman Bottles (SK3010) due to risk of stopper ejection causing injury.
Filters
Category
Agency
Severity
All Recalls
Back to home ←
CPSC•Residential Elevators StrikeLock Hoistway Door Locking DeviceResidential Elevators recalls StrikeLock hoistway door locking devices that may allow elevator cab movement with landing door open, risking serious injury or death.
CPSC•Segmart 4-Drawer DressersSegmart 4-Drawer Dressers (models FFLWM002BK, FFLWM002WE) recalled for tip-over and entrapment risk without wall anchoring.
FDA•MODERATEOphthavet Ophthalmic SolutionDechra is recalling Ophthavet Ophthalmic Solution for dogs and cats due to a lack of sterility assurance.
FDA•MODERATEAtomoxetine HCl 10mg CapsulesSafecor is recalling Atomoxetine HCl 10mg Capsules (NDC 64380-474-01) because some cartons may contain 25mg capsules due to a labeling error.
FDA•MODERATEPhilips Azurion and Allura Imaging SystemsPhilips is recalling Azurion and Allura imaging systems due to hard disk drive failure that may cause loss of functionality or data.
2 products
FDA•MODERATEHiResolution Bionic Ear SystemAdvanced Bionics is recalling the HiRes Ultra 3D CI HiFocus Mid Scala cochlear implant due to an incorrect shelf-life expiration date.
FDA•MODERATEBD Pyxis MedStation 4000 Fingerprint ScannerCareFusion 303 is recalling the BD Pyxis MedStation 4000 medication cabinet due to a fingerprint scanner overheating burn risk.
8 products
FDA•MODERATEDuloxetine Delayed-Release Capsules 30 mgAjanta Pharma is recalling Duloxetine Delayed-Release Capsules 30 mg due to the presence of an impurity exceeding FDA recommended limits.
3 products
FDA•MODERATEErythromycin 250 mg TabletsZydus is recalling Erythromycin 250 mg tablets due to CGMP deviations and the presence of an impurity above acceptable intake limits.
2 products
FDA•MODERATEProspector Popcorn Belgian Chocolate ToffeeProspector Popcorn Belgian Chocolate Toffee (UPC 850073852125) recalled for undeclared soy lecithin.
2 products
FDA•MODERATEPhilips Azurion Image-Guided Therapy SystemsPhilips is recalling various Azurion image-guided therapy systems due to mechanical wear that may impact table movement.
2 products- FDA•MODERATEPhilips Azurion X-Ray Tube Cooling Unit
Philips is recalling X-ray tube cooling units in Azurion systems due to hose degradation and potential oil leakage.
4 products 
FDA•MODERATEOasis Tears PF Lubricant Eye DropsOasis Tears PF eye drops (NDC 42126-6400-1) recalled due to lack of assurance of sterility.
FDA•MODERATEMetoprolol Succinate Extended-Release Tablets 25 mgAscend Laboratories is recalling 25 mg Metoprolol Succinate Extended-Release Tablets due to failed dissolution testing.
FDA•LOWPrimidone 50 mg TabletsGolden State Medical Supply is recalling Primidone 50 mg Tablets (NDC 51407-637-05) due to potential cross-contamination with Acemetacin.
2 products
FDA•MODERATEPhaseOne Antimicrobial Solution SprayerOculus Technologies is recalling PhaseOne Antimicrobial Solution due to sprayer spring corrosion that may contaminate the product.
FDA•MODERATECafe Nouria Blueberry MuffinThe Brownie Baker is recalling Cafe Nouria Blueberry Muffin due to undeclared walnuts, posing a risk to those with nut allergies.
FDA•MODERATEAligned Medical Fluids KitWindstone Medical Packaging is recalling the Aligned Medical AMS16835 Fluids Kit due to a supplier recall of the included Lidocaine injection.
FDA•MODERATEAmoxicillin and Clavulanate Potassium Oral Suspension DropsCronus Pharma is recalling Amoxicillin and Clavulanate Potassium oral suspension drops for dogs and cats due to product discoloration.
2 products
FDA•MODERATEOctreotide Acetate Injectable Suspension 30 mgTeva is recalling Octreotide Acetate 30 mg injectable suspension kits (NDC 0480-9262-08) due to sterility assurance concerns from manufacturing deficiencies.
2 products
FDA•MODERATEGood & Gather Sesame Teriyaki Chicken with RiceGood & Gather Sesame Teriyaki Chicken with Rice is recalled due to undeclared sesame and soy allergens.
- FDA•LOWPrimidone 250mg Tablets
Lannett Company is recalling Primidone 250mg Tablets (NDC 0527-1231-01) due to potential cross-contamination with Acemetacin API.
FDA•MODERATELiraglutide InjectionLupin is recalling Liraglutide Injection (NDC 70748-346-02 and 70748-346-03) due to white thread-like particulate matter in the cartridge.
FDA•MODERATEHydroMARK Breast Biopsy Site MarkerDevicor Medical is recalling HydroMARK breast biopsy site markers due to incorrect inner package labeling.
- Device RecallFDA•MODERATEGE HealthCare CARESCAPE Telemetry Server V5
GE HealthCare is recalling CARESCAPE Telemetry Server V5 units due to a risk of losing ECG and SpO2 monitoring capabilities.
6 products 
FDA•MODERATECASE v7.0 Cardiac Testing SystemGE Medical Systems is recalling the CASE v7.0 Cardiac Testing System due to a risk of electrical sparking and potential paper ignition.
FDA•MODERATEMedrad Avanta Injection System Tube SetsBayer is recalling Avanta Multi-Patient Administration Tube Sets due to a connection issue that may cause procedure interruptions.
FDA•MODERATEDa Vinci 5 NIR Handheld CameraIntuitive Surgical is recalling the da Vinci 5 NIR handheld camera system due to a risk of unintentional activation during surgery.
CPSC•AMZCMJ DGD Children's Tower StoolAMZCMJ DGD children's tower stools risk collapse, tipping, and child entrapment through side openings.
CPSC•TOETOL HOME Children's Tower StoolsTOETOL HOME tower stools (model DETD0001) can collapse or tip over, posing entrapment and fall hazards to children.
CPSC•Cpzzkq Baby LoungersCpzzkq baby loungers sold on Amazon pose suffocation risk; padding can obstruct infant breathing.
CPSC•KMUYSL Big Red Barn Farm Animal PlaysetsKMUYSL Big Red Barn Farm Animal Playsets (model SY-MZ7S-TVMV) recalled for detachable fence handles posing choking hazard to children under three.
CPSC•Magnetic Stick Figure SetsBlissfulDestiny magnetic stick figure sets recalled for loose magnets posing serious ingestion hazard to children.
CPSC•mGanna Sodium Hydroxide Pellet BagsmGanna Sodium Hydroxide pellet bags lack required child-resistant packaging, risking chemical burns and eye irritation.
CPSC•Autobrush Sonic Pro Kids Toothbrush BoxesAutobrush is recalling Sonic Pro Kids toothbrush boxes with accessible lithium coin batteries that pose serious ingestion hazards to children.
CPSC•32 Degrees Heated Socks32 Degrees heated socks (black, all sizes) recalled due to burn hazard during high-intensity activities.
CPSC•FitRx SmartBell Quick-Select Adjustable DumbbellsTzumi is recalling FitRx SmartBell dumbbells (model 8361) due to weight plates that can dislodge during use and cause serious injury.
CPSC•Sweetie Baby and Style Life Eleven Baby LoungersHappyGira recalls Sweetie Baby and Style Life Eleven baby loungers over fall and suffocation hazards violating infant sleep standards.
CPSC•Wiifo Children's Tower Stool Model LT005Wiifo tower stools (Model LT005) can collapse or tip, with side openings posing entrapment and fall risks to children.
FDA•MODERATEiVIZIA Sterile Lubricant Eye DropsThea Pharma is recalling iVIZIA Sterile Lubricant Eye Drops due to a lack of assurance of sterility.
2 products
FDA•MODERATECalypso Tropic Tango LemonadeKing Juice is recalling Calypso Tropic Tango Lemonade (16 fl oz) due to undeclared Yellow No. 5.
CPSC•LOWLil Pick Up Rex110 and Sierra110 Youth ATVsLil Pick Up recalls 4,900 Rex110 and Sierra110 youth ATVs over crash hazard, suspension defects, and burn risk from hot footwell surfaces.
FDA•MODERATEEnalapril Maleate Tablets, USP 20 mgRising Pharma is recalling Enalapril Maleate 20 mg tablets (NDC 64980-688-10) due to failed impurities test.
FDA•MODERATEJoint Nourish Liquid SupplementWellnov Supplements is recalling Joint Nourish liquid supplement due to potential bacterial contamination and C. botulinum concerns.
14 products
FDA•MODERATEOneLIF Interbody CageNovapproach Spine is recalling 60+ variants of OneLIF Interbody Cages due to a risk of inserter attachment failure during surgery.
2 products
FDA•MODERATESilastic Foley CathetersC.R. Bard is recalling Silastic Brand Foley Catheters due to surface staining on the devices.
FDA•MODERATECovidien Mon-a-Therm Esophageal StethoscopeCovidien is recalling Mon-a-Therm Esophageal Stethoscopes with Temperature Sensors because the devices lack FDA clearance.
3 products
FDA•MODERATEArvis Hip & Knee 3.0 Instrument Set ComponentsKico Knee Innovation is recalling Arvis Hip & Knee 3.0 instrument components over potential wear or corrosion on the magnet face.
2 products
FDA•MODERATESharpoint Microsurgical KnifeSurgical Specialties Corporation is recalling mislabeled Sharpoint microsurgical knives that contain 3.0mm blades instead of 2.2mm.