FDA•MODERATE
ICU Medical Oncology Extension Set
ICU Medical is recalling Oncology Extension Set REF: CL3960 due to a potential leak that could cause therapy interruption or hazardous exposure.
Filters
Category
Agency
Severity
All Recalls
Back to home ←
FSIS•MODERATEWhite Oak Pastures Grassfed Ground BeefWhite Oak Pastures Grassfed Ground Beef (16 oz) may contain metal; do not consume.
FDA•MODERATEBooey's Dragon's Breath SauceBooey's Dragon's Breath sauce is recalled for undeclared fish (anchovy) and sesame allergens.
FDA•MODERATEGentuity HF-OCT Imaging SystemGentuity is correcting the HF-OCT Imaging System (Model G10-01) to address a software issue that may cause inaccurate length measurements.
FDA•MODERATEOlympus Thunderbeat II ShearsOlympus is recalling Thunderbeat II Shears (Model TB2-0520FC) due to the risk of a distal tip component detaching during use.
4 products- Device RecallFDA•MODERATEGenius Digital Diagnostics System Review Station Display
Hologic is correcting Genius Review Station displays due to unauthorized configuration changes that deviate from validated settings.
FDA•MODERATEHiResolution Bionic Ear System M Zn-Air Battery PakAdvanced Bionics is recalling M Zn-Air Battery Paks for cochlear implants due to a non-compliant battery door design.
2 products
FDA•MODERATETangent Single Use Digital CatheterTangent Endoscopy is recalling single-use digital catheters due to a risk of fractures at the distal shaft tip.
FDA•MODERATEVancomycin HCl InjectionFagron is recalling Vancomycin HCl 1.5g/250mL injection due to sterility concerns and a potential detachment of the administration port part.
5 products
FDA•MODERATEExchange Select Honey Lemon Cough DropsExchange Select Honey Lemon Cough Drops are recalled due to manufacturing facility inspection observations that may impact product quality.
15 products
FDA•MODERATEFurosemide Tablets, USP 80 mgLeading Pharma is recalling Furosemide Tablets 80 mg (NDC 69315-118-01) due to N-nitroso-Furosemide above recommended limits.
FDA•MODERATEFoundationOne CDx Sequencing Agent SEQ0067Foundation Medicine is recalling Sequencing Agent SEQ0067 component of FoundationOne CDx due to possible false-positive BARD1 variants.
FDA•MODERATEProdisc C SK U.S. Cervical Disc ImplantCentinel Spine is recalling Prodisc C SK U.S. cervical disc implants due to a labeling mix-up between 5mm and 6mm sizes.
2 products
CPSC•Frigidaire Gas RangesFrigidaire is recalling 23 gas range models (serials VF52200000–VF54399999) due to delayed oven ignition posing a burn hazard.
CPSC•Amazon Basics Camping Folding Pocket KnifeAmazon Basics Camping Folding Pocket Knife (model B0DM5BJK3H) recalled due to blade mechanism failure and laceration hazard.
CPSC•Tainoki Fine Furniture Office ChairsTainoki is recalling office chairs (models M7016O, M7004O, M7074O) with bases that can bend, creating a fall hazard.
CPSC•Goregent Infant WalkerGoregent infant walkers (Model 901) sold on Amazon violate safety standards and pose fall hazards.
CPSC•Aisstxoer Adult Bicycle HelmetsAisstxoer model GH018L adult helmets (size large, pink) fail mandatory safety standards and may not protect in a crash.
CPSC•Specialized Turbo Como SL Electric Bicycle ForkSpecialized is recalling Turbo Como SL e-bike forks (2021–2026) due to fatigue crack risk causing fall hazard.
CPSC•Wagner 900 Series Power SteamersWagner is recalling 900 Series power steamers (models 905e, 915e, 925e) due to burn hazard from hot hose and water expulsion.
CPSC•BUILT LUUM Light Up TumblersBUILT LUUM light up tumblers (16–18 oz) recalled due to breakage exposing button cell batteries; choking and ingestion hazard to children.
FDA•MODERATERiverence Smoked Trout DipRiverence is recalling Smoked Trout Dip due to an undeclared milk allergen.
FDA•MODERATETramadol Hydrochloride Tablets, USP 50 mgAmneal is recalling tramadol 50 mg tablets (NDC 60219-2348-5) due to elevated N-nitroso-desmethyl-tramadol impurity.
FDA•MODERATEClonidine Transdermal System 0.2 mg/dayTeva Pharmaceuticals is recalling Clonidine Transdermal System 0.2 mg/day due to the use of an unapproved raw material during manufacturing.
3 products
FDA•MODERATECytal Wound Matrix 2-LayerIntegra LifeSciences is recalling Cytal Wound Matrix 2-Layer 5x5 cm dressings due to out-of-specification endotoxin results.
5 products- Device RecallFDA•MODERATEPhilips AneurysmFlow Software
Philips is recalling AneurysmFlow software due to unreliable MAFA ratio data that may lead to incorrect clinical decisions.
- Device RecallFDA•MODERATELeksell Vantage Arc System
Elekta is recalling the Leksell Vantage Arc System due to a defect in the locking mechanism that may cause coordinate shifting during procedures.
FDA•MODERATEMedline Neuro SpongesMedline is recalling various neuro sponges due to higher-than-expected endotoxin levels.
38 products
FDA•MODERATEDonJoy IceMan Classic3 Cold Therapy UnitDJO is recalling the IceMan Classic3 cold therapy unit (Model 11-0494) due to a broken connector that may interrupt cold therapy.
4 products
FDA•MODERATEDiversatek Healthcare Viper 3-Stage Fixed Wire Balloon DilatorDiversatek Healthcare is recalling the Viper 3-Stage Fixed Wire Balloon Dilator due to incorrect labeling of balloon sizes and pressures.
4 products
FDA•MODERATEBromfenac Ophthalmic Solution 0.07%Alembic Pharmaceuticals is recalling Bromfenac Ophthalmic Solution 0.07% (NDC 62332-583-03) due to failed impurities and degradation specifications.
FDA•MODERATEDimension Creatinine Flex Reagent CartridgeSiemens is recalling Dimension Creatinine Flex reagent cartridges (lots GA6307, BA7005) due to potential imprecision in patient creatinine results.
FDA•MODERATEOctreotide Acetate for Injectable SuspensionTeva is recalling Octreotide Acetate for Injectable Suspension due to a lack of assurance of sterility.
6 products
FDA•MODERATECurosurf (poractant alfa) 240 mg Intratracheal SuspensionChiesi USA is recalling Curosurf 240 mg intratracheal suspension vials (NDC 10122-510-03) due to lack of sterility assurance.
FDA•MODERATEXanax XR Alprazolam 3 mg TabletsViatris is recalling Xanax XR 3 mg tablets (NDC 58151-506-91) due to failed dissolution specifications.
FDA•MODERATEStraumann Custom Abutment TiStraumann is recalling custom abutments manufactured with incorrect raw material.
2 products
FDA•MODERATEAlbuterol Sulfate Inhalation Solution 0.5%Nephron SC recalling Albuterol Sulfate Inhalation Solution (NDC 69374-330-05) due to illegible labeling.
FDA•MODERATELucerne 2% Cottage CheeseAlbertsons is recalling Lucerne 2% Cottage Cheese due to potential contamination with metal fragments.
FDA•MODERATEMeclizine Hydrochloride Tablets 12.5 mgAmerican Health Packaging is recalling Meclizine Hydrochloride 12.5 mg tablets (NDC 60687-775-65 and 60687-775-11) due to failed tablet specifications.
FDA•MODERATECinacalcet Hydrochloride TabletsCipla is recalling Cinacalcet Hydrochloride Tablets due to the presence of N-Nitroso Cinacalcet above acceptable limits.
3 products
FDA•MODERATEMedline CENTURION Circumcision KitMedline is recalling CENTURION Circumcision Kit (CIT7050F) due to one lot distributed without sterilization.
FDA•MODERATEAccess Total T4 CalibratorBeckman Coulter is recalling Access Total T4 Calibrator (Catalog No. 33805) due to negative bias causing falsely low results on DxI 600/800 instruments.
FDA•MODERATEFlamingo Funnel SmallSurgiSmoke Solutions is recalling the Flamingo Funnel Small due to a manufacturing error involving non-gamma compatible sterilization drapes.
3 products
FDA•MODERATEMedline Universal Central/Art Line Insertion KitMedline is recalling convenience kits containing non-sterile alcohol prep pads due to potential bacterial contamination.
10 products
FSIS•MODERATELa Boulangerie Turkey Pesto & Swiss Cheese PocketsLa Boulangerie Turkey Pesto & Swiss Cheese Pockets (25.4 oz, lot 04926) may contain mislabeled ham and cheese filling instead of turkey, pesto, and cheese.
FDA•MODERATELanreotide Injection 120 mg/0.5 mLCipla is recalling Lanreotide Injection 120 mg/0.5 mL due to a lack of assurance of sterility.
2 products
FDA•MODERATENoromycin 300 LA Oxytetracycline InjectionMWI Animal Health is recalling Noromycin 300 LA oxytetracycline injection (NADA# 141-143) due to lack of assurance of sterility.
FDA•MODERATEMagellan Diagnostics LeadCare II Blood Lead Test KitsMagellan Diagnostics is recalling LeadCare II blood lead test kits due to the risk of false positive results.
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.
CPSC•17 Stories Furniture 14-Drawer Dressers17 Stories 14-Drawer Dressers recalled for tip-over and entrapment hazards; wall anchoring required. Models 55SCDR14KD* sold via Wayfair Sept 2023–Jan 2026.