FDA•MODERATE
EXCOR Pediatric VAD Blood Pump PU Valves
Berlin Heart is recalling EXCOR Pediatric VAD Blood Pump PU Valves due to an expiration date mismatch that could delay surgical procedures.
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FDA•MODERATESporeTraq Mail-In Spore Testing ServiceSporeTraq Mail-In Spore Testing Service recalled due to incorrect incubation process; model 1023780.
4 products
FDA•CRITICALHaleon US: multiple softgelsHaleon recalls Gas-X Extra Strength softgels (120 & 72 ct) over possible coolant contamination.
2 products
FDA•CRITICALPearl Milling Original Pancake & Waffle Mix CompletePearl Milling pancake mix recalled for undeclared milk and soy allergens.
FDA•CRITICALup & up Fragrance Free Baby WipesTarget is recalling up & up Fragrance Free Baby Wipes due to potential contamination with Burkholderia cepacia and Burkholderia gladioli.
2 products
CPSC•Gudook Bicycle HelmetsGudook-branded bicycle helmets are recalled for failing to meet federal safety standards, posing a serious risk of head injury.
CPSC•Crenlux Pool Drain CoversCrenlux pool drain covers are recalled due to entrapment and drowning hazards that violate federal safety standards.
CPSC•Little Grape Land Nursing PillowsLittle Grape Land nursing pillows are recalled due to a suffocation hazard and failure to meet federal safety standards.
CPSC•Broqixin Pool Drain CoversBroqixin pool drain covers (Model 11064W) are recalled for failing to meet federal entrapment protection standards, posing a drowning hazard.
CPSC•SUNS International Residential Elevator Interlock SwitchesSUNS International is recalling residential elevator interlock switches that can fail to lock, posing a fall and crushing hazard.
CPSC•Tiny Land Children's Play TentsTiny Land children's play tents are recalled due to fiberglass poles that can shed fibers, posing a risk of skin and eye irritation.
CPSC•Boon NURSH 8 oz Reusable Baby BottlesBoon NURSH 8 oz baby bottles are recalled due to a choking hazard from peeling plastic shell pieces.
CPSC•Vornado Small Room Tower HeatersVornado is recalling SRTH small room tower heaters due to a fire hazard caused by fan blades detaching and the unit overheating.
CPSC•Wyze Solar Cam Pan Security CamerasWyze is recalling Solar Cam Pan security cameras (Model WYZESCPWH) due to a fire and burn hazard from potential battery puncture.
FDA•MODERATESiemens ARTIS pheno X-ray SystemSiemens recalls ARTIS pheno X-ray system over dose display error.
2 products
FDA•CRITICALThe Coffee Connexion: 4 Poly Bag And PackedsCheese sauce mixes and related products recalled over potential Salmonella from dry milk powder.
4 products
FDA•CRITICALDraeger Atlan A350 Anesthesia WorkstationDraeger recalls Atlan A350 anesthesia workstation due to piston ventilator failure risk.
2 products
FDA•MODERATESharpoint Microsurgical KnifeSurgical Specialties Corporation is recalling Sharpoint microsurgical knives mislabeled as 2.2mm when they are actually 3.0mm.
FDA•CRITICALKayserBett IDA Pediatric Care BedKayserBett is recalling the IDA pediatric care bed due to an entrapment risk if the hand control is not locked while the child is unattended.
FDA•MODERATEGrace Medical Stapes ProsthesisGrace Medical is recalling the Titanium/Fluoroplastic Piston Stapes Prosthesis due to incorrect functional length listed on the labeling.
FDA•MODERATEDa Vinci 5 NIR Handheld CameraIntuitive Surgical is recalling the da Vinci 5 NIR handheld camera system due to a risk of unintentional illumination activation.
2 products
FDA•MODERATENiacin Extended-release Tablets 1,000 mgLannett is recalling Niacin Extended-release Tablets 1,000 mg due to failed dissolution specifications.
FDA•MODERATEKirkland Signature Ultra Strength AntacidKirkland Signature antacid recalled due to metallic particles in tablets.
23 products
FDA•MODERATEXyvona (levorphanol tartrate) 2mg TabletsForte BioPharma recalls Xyvona (levorphanol tartrate) 2mg tablets due to FDA denial of proprietary name.
2 products
FDA•CRITICALRaw Shelled Peanuts (Runner Type)Wilco Peanut Co. is recalling raw shelled peanuts due to an undeclared tree nut allergen.
FDA•MODERATEDeRoyal Covaderm Plus Vascular Access DressingDeRoyal is recalling Covaderm Plus Vascular Access Dressing (Ref 46-406) due to a lack of sterility assurance.
FDA•MODERATEAligned Medical Fluids KitWindstone Medical Packaging is recalling Aligned Medical AMS16835 Fluids Kits due to a supplier recall of the included Lidocaine injection.
- Device RecallFDA•CRITICALIvenix Infusion System LVP Software
Fresenius Kabi is recalling Ivenix Infusion System LVP software due to a potential battery-health reporting error that may cause pump shutdown.
FDA•MODERATEGE MAC 5 A4 and A5 Resting ECG Analysis SystemsGE is recalling MAC 5 A4 and A5 ECG systems due to a software error that may incorrectly associate clinical data with the wrong patient.
FDA•MODERATEBD Pyxis MedStation 4000 Fingerprint ScannerBD Pyxis MedStation 4000 recalled: fingerprint scanner may overheat, causing burns.
8 products
FDA•MODERATEMedrad Avanta Injection System Tube SetsBayer is recalling Avanta Multi-Patient Administration Tube Sets due to a fit issue that may cause connection instability during use.
FDA•CRITICALPencan Spinal Needle TraysB. Braun recalls Pencan spinal needle trays over potential quality issues with bupivacaine component.
6 products
FDA•CRITICALDried Herring FishPrime Food is recalling 7 oz. Dried Herring Fish due to potential Clostridium botulinum contamination from improper evisceration.
FDA•MODERATEStandard Pasteurized Donor Human MilkUC Health Milk Bank recalls donor human milk bottles over possible plastic particle contamination.
FDA•MODERATELidocaine HCl Injection USPSpectra Medical Devices is recalling Lidocaine HCl Injection USP single-dose ampules due to a lack of assurance of sterility.
FDA•MODERATELunds & Byerly's Curry Powder SweetLunds & Byerly's Curry Powder Sweet is recalled due to undeclared sesame seeds in the product.
- Food RecallFDA•MODERATEAlbertsons: multiple undeclared allergens
121 Albertsons products recalled for undeclared tree nuts, fish, or shellfish.
121 products 
FDA•MODERATEAmlodipine and Olmesartan Medoxomil TabletsAscend Laboratories is recalling Amlodipine and Olmesartan Medoxomil Tablets, 5mg/40mg, due to failed dissolution specifications.
FDA•MODERATEArvis Hip & Knee 3.0 Instrument SetKico recalls Arvis Hip & Knee 3.0 Instrument Set over magnet face wear/corrosion.
2 products
FDA•MODERATEShimadzu X-Ray Systems High Voltage GeneratorShimadzu recalls X-ray systems over generator contactor weld risk; full model list on FDA page.
2 products
FDA•MODERATEDuloxetine DR Capsules 30 mgAsclemed USA is recalling Duloxetine DR Capsules 30 mg due to the presence of a nitrosamine impurity above acceptable intake limits.
FDA•MODERATEPhaseOne Antimicrobial Solution SprayerOculus Technologies is recalling PhaseOne Antimicrobial Solution due to sprayer spring corrosion that may contaminate the product.
FDA•MODERATECASE v7.0 Cardiac Testing SystemGE Medical is recalling the CASE v7.0 Cardiac Testing System due to a risk of electrical sparking at the printer head.
FDA•MODERATEHiRes Ultra 3D CI HiFocus Mid Scala Cochlear ImplantAdvanced Bionics is recalling the HiRes Ultra 3D CI HiFocus Mid Scala cochlear implant due to an incorrect shelf-life expiration date.
2 products
FDA•MODERATENeptune Smart Docking StationStryker is recalling the Neptune Smart Docking Station (120V) due to missing safety testing and a potential electrical shock risk.
FDA•MODERATECovidien EndoStitch Polysorb Single Use Loading UnitCovidien is recalling EndoStitch Polysorb loading units (170053, 170071) due to packaging holes that may compromise sterility.
FDA•MODERATEMotor City Pizza Co. 5 Cheese BreadMotor City Pizza Co. 5 Cheese Bread recalled over potential Salmonella contamination.
FDA•Udder Products Yeast BlendNutra Blend is recalling 50 lb bags of Udder Products Yeast Blend due to elevated selenium levels.
FDA•CRITICALGuittard 72% Cacao Chocolate with Date Sugar WafersGuittard is recalling 25lb bulk containers of 72% Cacao Chocolate with Date Sugar Wafers due to potential Salmonella contamination.
FDA•CRITICALIvenix Large Volume PumpFresenius Kabi is recalling Ivenix Large Volume Pumps due to potential touchscreen malfunctions caused by internal damage from drops or jarring.