FDA•LOW
Pitavastatin Tablets, 2 mg
Northstar Rx LLC is recalling Pitavastatin Tablets, 2 mg (NDC 72603-479-01) due to a foreign 1 mg tablet found in bottles.
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All Recalls
Back to home ←- Device RecallFDA•MODERATECentricity Universal Viewer Software
GE recalls Centricity Universal Viewer software over credential exposure risk.
4 products 
FDA•CRITICALBlue Bull Extreme Male Enhancement SupplementBlue Bull Extreme Male Enhancement recalled due to undeclared sildenafil.
3 products
CPSC•Playground Swing Set SeatsPlayground swing seats (model 999604) are being recalled due to a fall hazard caused by potential rivet failure.
FDA•MODERATEID NOW Influenza A & B 2 Test KitAbbott is recalling ID NOW Influenza A & B 2 test kits (Model 427-000) due to an increased rate of invalid results.
FDA•CRITICALOmnipod 5 PodsInsulet is recalling Omnipod 5 Pods due to a cannula defect that can cause insulin under-delivery and severe health risks.
FDA•Favorina Chocolate LadybugsLidl recalls Favorina Chocolate Ladybugs over undeclared hazelnuts; return for refund.
CPSC•17 Stories 14-Drawer Dressers17 Stories 14-Drawer dressers are recalled due to tip-over and entrapment hazards that violate federal safety standards.
CPSC•ProRider Bicycle HelmetsProRider is recalling various bicycle helmets that fail federal safety standards, posing a serious risk of head injury or death in a crash.
CPSC•LIVEHOM 11-Drawer DressersLIVEHOM 11-Drawer Dressers are recalled due to tip-over and entrapment hazards that pose a risk of serious injury or death to children.
CPSC•Kluster Magnet Chess GamesStoney Games is recalling Kluster magnet chess games due to a serious magnet ingestion hazard that can cause severe internal injury or death.
FDA•MODERATEMedline Cardiac Procedure KitsMedline is recalling cardiac procedure kits to clarify that the included chest drainage units are intended for adult patients only.
FDA•MODERATEMedline Medcrest Surgical GownsMedline is recalling Medcrest surgical gowns due to fabric delamination risks that may lead to infection or delays in patient care.
3 products
FDA•MODERATELutronic CLARITY II Laser SystemLutronic is recalling CLARITY II Laser System (Model 1110200210) due to sparking and burn hazard.
FDA•Primal Herbs VolumePrimal Herbs Volume recalled for undeclared sildenafil; may lower blood pressure dangerously.
FDA•MODERATECocos Wholesale and Imports: 2 productsCoco's Italian Market recalls Cannoli Making Kit and Fettuccini Alfredo for undeclared wheat and milk allergens.
2 products
FDA•CRITICALKarns Foods Mini Dark Chocolate Raspberry CupsKarns Foods is recalling Mini Dark Chocolate Raspberry Cups due to undeclared peanuts.
FDA•CRITICALLobster & Crab RavioliPerfect Pasta is recalling Lobster & Crab Ravioli due to undeclared shrimp, crab, lobster, pollock, whiting, and soy allergens.
FDA•MODERATETemozolomide Capsules 5mgRising Pharmaceuticals is recalling Temozolomide Capsules 5mg (NDC 16571-816-51) due to failed impurities and degradation specifications.
FDA•MODERATESemaglutide Injection 2 mg Multi-Dose VialsNew Life Pharma recalls semaglutide 2 mg vials over sterility concerns.
4 products
FDA•MODERATEAmnesteem Isotretinoin Capsules 40 mgMylan is recalling Amnesteem Isotretinoin 40 mg capsules (NDC 0378-6614-93) due to failed dissolution specifications.
FDA•MODERATESodium Iodide (I-131) Therapeutic Oral SolutionRadnostix is recalling Sodium Iodide (I-131) Therapeutic Oral Solution due to the presence of particulate matter.
FDA•MODERATEArtelon FlexBand Dynamic MatrixArtelon FlexBand Dynamic Matrix recalled over failed endotoxin testing.
3 products
FDA•MODERATEBeckman Coulter DxC 700 AU Chemistry AnalyzerBeckman Coulter recalls DxC 700 AU and AU5800 analyzers over software delay risk.
2 products- Device RecallFDA•MODERATEHealthCast Vital Sync Remote Patient Monitoring System
HealthCast is recalling Vital Sync software due to a failure to transmit or receive critical patient bedside monitor alarms.
2 products 
FDA•MODERATEEndoVive Safety PEG KitBoston Scientific is recalling EndoVive Safety PEG Kits due to compromised seals on the included antiseptic swabsticks.
FDA•MODERATELowes Foods Sour Cream and Onion Potato ChipsUncle Ray's recalls Lowes Foods sour cream & onion chips (8 oz) over inaccurate nutrition and undeclared MSG.
FDA•MODERATEEndo-Model Replacement PlateauEndo-Model Replacement Plateau is recalled due to a risk of bushing detachment from the screw shaft caused by longitudinal fractures.
13 products
FDA•MODERATEGEM Premier 5000 PAKInstrumentation Laboratory is recalling GEM Premier 5000 PAK cartridges due to errors that may cause ejection and delay patient results.
20 products
FDA•MODERATEPhysio-Control Infant/Child Defibrillator ElectrodesPhysio-Control is recalling infant/child defibrillator electrodes due to a risk of delamination that could impact therapy delivery.
2 products
FDA•MODERATEAPTUS 2.5 TriLock ScrewsMedartis is recalling APTUS 2.5 TriLock Screws (model A-5750.16/1) due to a mix-up with 2.8mm screws.
2 products
FDA•MODERATEVegetarian Chicken Flavor RamenPalmetto Gourmet Foods is recalling Vegetarian Chicken Flavor Ramen 3oz packages due to undeclared Yellow #5.
2 products
FDA•MODERATEEquinoxe Core Instrument KitExactech recalls Equinoxe Core Instrument Kit and Ergo Impactor Handle over missing cross-pin risk.
2 products
FDA•LOWC2O Coconut Water with Pulp 17.5 ozC2O Coconut Water with Pulp 17.5 oz recalled over incorrect outer box labeling omitting added sugar.
FDA•MODERATERaz Mobile Shower Commode ChairsRaz Design is recalling various mobile shower commode chairs due to a seat bracket issue that may pose a fall risk to users.
2 products
FDA•MODERATEMedline Unna-Z Stretch Zinc Paste BandageMedline is recalling Unna-Z Stretch Zinc Paste Bandages due to an incomplete ingredient list on the label.
FDA•MODERATEBD 10mL Non-Sterile Luer-Lok SyringeBD is recalling 10mL non-sterile Luer-Lok syringes (catalog 301029) due to incorrect Luer Slip syringes mixed into batches.
FDA•MODERATEIBA Proton Therapy System PROTEUS 235IBA PROTEUS 235 proton therapy systems may fail to stop beam delivery if external gating device signal is lost, risking patient mistreatment.
CPSC•Tomum Minoxidil Hair Growth TreatmentTomum Minoxidil Hair Growth Treatment is recalled because the non-child-resistant packaging poses a poisoning risk to young children.
CPSC•Cubimana Island Storm 3-in-1 Building SetsCubimana Island Storm building sets (Model HG1004) are recalled because the LED light's battery compartment poses a serious ingestion hazard.
CPSC•Forever 21 Kids Disney Mickey Mouse Pajama PantsForever 21 Kids Disney Mickey Mouse Pajama Pants are recalled for violating federal flammability standards, posing a serious burn hazard.
CPSC•HALO Magic SleepsuitsHALO is recalling Magic Sleepsuits due to a choking hazard from detachable zipper heads.
FDA•MODERATEHTO Nevada: Multiple Dermal Source ProductsKirkman recalls Vasocaine Spray and Zone 1/2 Lidocaine Creams over unsupported expiry dates.
3 products
FDA•MODERATEOlympus ShockPulse-SE Lithotripsy System GeneratorOlympus is recalling the ShockPulse-SE Lithotripsy System generator due to a wiring issue that may cause treatment delays.
2 products
FDA•Miss Vickie's Spicy Dill Pickle Potato ChipsFrito-Lay recalls Miss Vickie's Spicy Dill Pickle chips (8 oz.) over undeclared milk allergen.
FDA•MODERATEVergani Pandoro Classico Gluten FreeVergani Pandoro Classico Gluten Free recalled due to possible Teflon fragments.
FDA•MODERATEMedline Nail KitMedline is recalling the Nail Kit (model DYKM1528) because the included sterile saline wound wash may not meet sterility requirements.
5 products
FDA•MODERATEBader Enterprises: 2 Clear Flexible Plastic PackagingsBader Enterprises recalls Premium Food Jordan Almonds and Bubble Gum for undeclared wheat and FD&C Blue 1 & 2 Lake.
2 products
FDA•LOWCipla: Multiple Packaged In Cartons CapsulesCipla recalls Nilotinib 150 mg and 200 mg capsules over failed specification tests.
2 products
FDA•MODERATEMidodrine Hydrochloride Tablets, USP 5 mgMajor Pharmaceuticals is recalling Midodrine Hydrochloride Tablets 5 mg (NDC 0904-6818-06) due to inadequately sealed blister packaging.