CPSC•
LiCB Lithium Coin Batteries
LiCB CR2032 lithium coin batteries are recalled for lacking child-resistant packaging and warning labels, posing a severe ingestion hazard.
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CPSC•Misco Sports Badminton Toy SetsMisco Sports badminton toy sets are recalled due to a battery ingestion hazard from easily accessible button cell batteries in the shuttlecock.
CPSC•Petzl SIMBA and SWAN EASYFIT HarnessesPetzl is recalling SIMBA and SWAN EASYFIT harnesses due to a buckle defect that poses a serious fall hazard.
CPSC•Superbobi Pool Drain CoversSuperbobi pool drain covers are recalled for failing to meet safety standards, posing entrapment and drowning hazards to swimmers.
CPSC•Tiyol Pull String Teething ToysTiyol pull string teething toys (Model 688-59) are recalled due to a choking hazard from strings that can lodge in a child's throat.
CPSC•Zwilling Enfinigy Electric KettlesZwilling is recalling Enfinigy electric kettles because the handle can detach, posing a burn hazard from hot contents.
FDA•CRITICALDOXOrubicin Hydrochloride Liposome InjectionSun Pharma recalls DOXOrubicin Liposome Injection 50 mg/25 mL vials due to glass particulate matter.
FDA•MODERATECodman CerebroFlo EVD CatheterIntegra LifeSciences is recalling the Codman CerebroFlo EVD Catheter due to out-of-specification endotoxin results.
FDA•CRITICALArrow Edge Hemodialysis Catheterization ProductArrow Edge hemodialysis catheterization product recalled: sheath introducer may not split, risking injury.
6 products
FDA•MODERATEBARD Dynamic Deca Steerable CatheterBARD Dynamic Deca Steerable EP catheter recalled due to incomplete seals on sterile product.
26 products
FDA•MODERATEEdwards EVOQUE Tricuspid Delivery SystemEdwards Lifesciences is updating the labeling for the EVOQUE tricuspid delivery system to include a warning about potential functionality issues.
FDA•MODERATECreamy Sesame NoodlesFly By Jing recalls Creamy Sesame Noodles over possible undeclared peanut allergen.
FDA•MODERATEZYMUTEST HIA IgG ELISA KitZYMUTEST HIA IgG ELISA kit lot FD1265 distributed with outdated flyer containing incorrect positive control values.
FDA•MODERATEPhilips Azurion Cable Hose CarrierPhilips is recalling Azurion imaging systems due to potential loosening or breakage of Cable Hose Carrier bolts and plastic parts.
FDA•MODERATEQuickVue Dipstick Strep A TestQuidel is recalling QuickVue Dipstick Strep A Test (REF 20108) due to risk of false positive results.
FDA•MODERATEThermedx FluidSmart Urology Tube SetStryker is recalling the FluidSmart Urology Tube Set (REF LL0006) due to the distribution of nonconforming products.
FDA•MODERATESelenia Dimensions Mammography SystemsHologic recalls Selenia Dimensions mammography systems over loose or broken internal bolts.
2 products
FDA•MODERATEMetoprolol Succinate Extended-Release Tablets 25 mgAscend Laboratories is recalling 25 mg Metoprolol Succinate Extended-Release Tablets due to failed dissolution testing.
FDA•MODERATEDexcom G7 CGM iOS AppDexcom recalls G7 CGM iOS App (v2.9.0–2.11.2) over glucose alert delays that may cause missed hypo/hyperglycemic events.
4 products
FDA•MODERATEBuprenorphine Hydrochloride Injection 0.3mg/mLEndo USA recalls Buprenorphine Hydrochloride Injection 0.3mg/mL vials (NDC 42023-179-05) due to particulate matter contamination.
FDA•MODERATEDiowave 250W Laser SystemDiowave 250W Laser System recalled; software update needed to correct power output exceeding FDA-cleared 60W limit.
FDA•MODERATELUCAS Chest Compression SystemJolife AB is recalling LUCAS 2, 3, and 3.1 chest compression systems due to missing service documentation.
2 products
FDA•CRITICALMG217 Multi-Symptom Treatment CreamMG217 Multi-Symptom Treatment Cream recalled due to Staphylococcus aureus contamination.
FDA•MODERATEOasis Tears PF Lubricant Eye DropsOasis Tears PF eye drops (NDC 42126-6400-1) recalled due to lack of assurance of sterility.
FDA•MODERATEDakota Honey: 5 CompaniesDakota Honey recalls Spreadable Spun Honey varieties over possible metal/plastic contamination.
5 products
FDA•MODERATERevolution Ascend CTGE HealthCare recalls Revolution Ascend CT over AW Server security vulnerability.
7 products
FDA•CRITICALNamic Angiographic ManifoldMedline recalls Namic Angiographic Manifolds (SKU 64038200) due to particulate in the fluid path.
14 products
FDA•MODERATEDonJoy IceMan Classic CubeDonJoy IceMan Classic Cube recalled due to broken connector interrupting cold therapy.
4 products
FDA•CRITICALGeorge J Howe: 6 productsGeorge J Howe recalls sunflower seed products due to undeclared cashew allergen.
6 products
CPSC•Analemma Water BottlesAnalemma is recalling 24 oz stainless-steel water bottles due to a risk of serious injury or death from glass liner breakage.
CPSC•EEMB Lithium Coin BatteriesEEMB is recalling lithium coin batteries in non-child-resistant packaging, posing a serious ingestion and chemical burn hazard to children.
CPSC•Favoto Bicycle HelmetsFavoto is recalling Model H-1 bicycle helmets because they fail to meet federal safety standards, posing a serious head injury risk.
CPSC•Foubeaka and Geniuss Multi-Purpose HelmetsFoubeaka and Geniuss multi-purpose helmets are recalled for failing to meet federal safety standards, posing a risk of serious head injury.
CPSC•Rublev Colours Gum Turpentine and Mineral SpiritsNatural Pigments is recalling Rublev Colours Gum Turpentine and Mineral Spirits due to missing child-resistant packaging and poisoning risks.
CPSC•Justforjoyful Rainbow Wall ToysJustforjoyful Rainbow Wall Toy (model JJ1602) is recalled due to a choking hazard posed by the xylophone drumstick.
CPSC•Svnntaa Adult Portable Bed RailsSvnntaa adult portable bed rails are recalled due to serious entrapment, asphyxiation, fall, and laceration hazards.
CPSC•ZMC Group Light Up ToysZMC Group is recalling various light-up toys due to a risk of serious injury or death from accessible button cell batteries.
FDA•MODERATEBioCera Fibers Bone Void FillerOrthorebirth recalls BioCera Fibers bone void filler (REFs ORB-0320C-KC, ORB-0310C-KC, ORB-0304C-KC, ORB-0302C-KC, ORB-0305D-KC) for out-of-spec.
2 products
FDA•MODERATEMedline Convenience KitsMedline is recalling Ancillary Pack-LF and Open Heart Anesthesia ICC-A kits due to potential issues with sterilization and packaging calibration.
58 products
FDA•MODERATEDuloxetine Delayed-Release Capsules 60mgBreckenridge Pharmaceutical is recalling Duloxetine 60mg capsules distributed nationwide due to the presence of an impurity above FDA limits.
FDA•MODERATENaproxen Oral SuspensionAcella Pharmaceuticals is recalling Naproxen Oral Suspension, 125 mg/5mL, distributed nationwide due to lead and lithium contamination.
FDA•MODERATEBioFire Joint Infection PanelBioFire is recalling the Joint Infection (JI) Panel due to contamination that may cause false positive test results.
- Device RecallFDA•MODERATEMint Lesion Software
Mint Medical is recalling Mint Lesion software versions 3.4.0–3.9.5 due to a risk of data loss or incorrect patient information linking.
FDA•MODERATEOne Step 10A in vitro diagnostic testOne Step 10A in vitro diagnostic test recalled for lack of FDA clearance.
7 products
FDA•MODERATEBiofire Spotfire Respiratory/Sore Throat PanelBioFire is recalling the Spotfire Respiratory/Sore Throat Panel due to the risk of false negative results and control failures.
FDA•MODERATEDEX Ophthalmic Tissue ForcepsKatalyst Surgical recalls DEX Ophthalmic Tissue Forceps, model DVF4005-23, due to IFU corrective action.
12 products
FDA•MODERATEJesse Withrow: 2 Glass Mason Jars With Metal LidsMy Wife's Slaw (original and Jalapeno Heat) recalled for lack of approved food establishment inspection.
2 products
FDA•CRITICALJOHN B SANFILIPPO & SONS: 6 productsJohn B. Sanfilippo recalls nut mixes over Salmonella risk.
6 products
FDA•MODERATEWoodstock Organic Shelled EdamameWoodstock Organic Shelled Edamame recalled over possible metal pieces.
FDA•MODERATEOctreotide Acetate for Injectable SuspensionTeva is recalling Octreotide Acetate 30 mg injection kits due to a lack of assurance of sterility.
2 products