FDA•MODERATE
Cub Pediatric Crib Model FL19H
Stryker is recalling Cub Pediatric Crib Model FL19H over missing access door warning labels.
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FDA•MODERATESTA Liatest D-Di Assay KitDiagnostica Stago is recalling the STA Liatest D-Di kit due to a positive bias in D-Dimer measurements that may cause inaccurate test results.
2 products
FDA•MODERATEWillamette Valley Pie: 4 productsWillamette Valley recalls frozen raw Blueberry Crumble Pies (8" & 9") over possible Listeria contamination.
4 products
FDA•MODERATEBlueFrog Foods: 2 For Green Way Farms Of Georgia GasGreenway Farms recalls Garlic and Jalapeno Dill Pickle Chips (16 fl oz) over lack of process authority.
2 products
FDA•MODERATECNC Noodle: 4 Carbonate And Benzoate Of Soda Added AsCNC Noodle recalls Steam Noodles and Zhong Hua Chao Mian Noodles due to undeclared wheat.
4 products
FDA•MODERATEHortex Spring Vegetable MixHortex Spring vegetable mix is being recalled due to potential contamination with glass.
FDA•MODERATETETAS Mireya Cherry Milkshake PopsicleTETAS Mireya Cherry Milkshake popsicles recalled for undeclared soy lecithin allergen.
FDA•MODERATEIcosapent Ethyl CapsulesZydus Pharmaceuticals is recalling Icosapent Ethyl Capsules due to oxidation, which can cause capsule melting and discoloration.
FDA•MODERATEWelch Allyn Spot Vision Screener VS100Welch Allyn is recalling the Spot Vision Screener VS100 (software v3.2.0.1) due to a screen flickering issue that may trigger seizures.
FDA•MODERATEBioCox 60 Type A Medicated ArticleHuvepharma is recalling BioCox 60 Type A Medicated Article due to failure to meet stability specification requirements.
FDA•MODERATESimply Nature Spinach BitesDr. Praeger's is recalling Simply Nature Spinach Bites (12 oz) due to possible rodent hair contamination.
FDA•MODERATEChildren's Ibuprofen Oral Suspension 100 mg/5mLTaro Pharmaceuticals is recalling Children's Ibuprofen Oral Suspension 100 mg/5mL (120 mL) due to gel-like masses and black particles.
- Device RecallFDA•MODERATECentricity Universal Viewer Software
GE recalls Centricity Universal Viewer software over credential exposure risk.
4 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.
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•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•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•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•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