FDA•MODERATE
Grace Medical Stapes Prosthesis
Grace Medical is recalling the Titanium/Fluoroplastic Piston Stapes Prosthesis due to incorrect functional length listed on the labeling.
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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•LOWYunker Energy & Health Herbal SupplementSato Pharmaceutical is recalling Yunker Energy & Health Herbal Supplement due to a failure to meet label claims for Vitamin E content.
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.
FSIS•CRITICALSynear Supreme Soup Dumplings Pork & CrabSynear Foods recalls 71,603 lbs of frozen pork & crab soup dumplings due to undeclared peanut allergen.
3 products
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•LOWLidocaine HCl Injection 2%Eugia US LLC is recalling Lidocaine HCl Injection 2% because the label wrap covers the barcode, making it difficult to scan.
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.
- Device RecallFDA•MODERATEB. Braun CESK Northside Anesthesia Tray
B. Braun recalls CESK Northside Anesthesia Tray due to cracked adhesive tubing.
8 products 
FDA•MODERATECovidien Mon-a-Therm Esophageal StethoscopeCovidien recalls Mon-a-Therm Esophageal Stethoscope 400TM (REF 90042) due to lack of FDA clearance.
3 products
FDA•MODERATEExacta Mix Vented Micro-Volume InletBaxter is recalling Exacta Mix Vented Micro-Volume Inlet (Model H938175) due to incorrect filters that may cause flow and clinical issues.
FDA•CRITICALBD Spinal Tray with Quincke NeedleBD recalls Spinal Tray with Quincke Needle over quality issues in bupivacaine component.
10 products
FDA•MODERATECovidien Shiley Tracheostomy TubeCovidien is recalling Shiley Tracheostomy Tubes due to incorrect display box labeling.
FDA•MODERATEIvenix Infusion System Large Volume PumpFresenius Kabi is recalling the Ivenix Infusion System LVP due to a risk of the cassette loading lever breaking during use.
FDA•MODERATEGE HealthCare CARESCAPE Telemetry ServerGE HealthCare recalls CARESCAPE Telemetry Server V5 ATO over potential loss of ECG and SpO2 monitoring.
6 products
FDA•MODERATEMedtronic 1x4 Pocket Adaptor KitMedtronic recalls 1x4 Pocket Adaptor Kit (Model 64001) due to incorrect Use-By-Dates.
2 products
FDA•MODERATEMedline Eye Tray-LF Convenience KitMedline is recalling Eye Tray-LF kits containing mislabeled Cardinal Health syringes that may lead to incorrect insulin dosing.
FDA•CRITICALMedline Anesthesia Trays with Huons BupivacaineMedline recalls anesthesia trays with Huons bupivacaine over quality and efficacy issues.
10 products
FDA•MODERATEPhilips Azurion System HDDPhilips recalls Azurion systems over aging HDDs that may cause loss of imaging or movement.
3 products
FDA•Better Weather Fix ElixirBetter Weather recalls Fix Elixir 15ml due to undeclared Kratom derivative (MP).
FDA•CRITICALDark Chocolate Coconut Almond BitesBazzini recalls Dark Chocolate Coconut Almond Bites over undeclared peanuts.
FDA•CRITICALD'Dioses Fruit Pops: multiple undeclared allergens32 D'Dioses Fruit Pops products recalled for undeclared tree nuts or milk.
32 products
FDA•LOWPred Mild Ophthalmic SuspensionAbbVie is recalling 10 mL bottles of Pred Mild ophthalmic suspension due to failed stability specifications.
FDA•MODERATEHydroMARK Breast Biopsy Site MarkerDevicor Medical is recalling HydroMARK breast biopsy site markers due to incorrect inner package labeling.