FDA•MODERATE
Second Nature Keto Crunch Smart Mix
Second Nature is recalling Keto Crunch Smart Mix due to undeclared cashews, pistachios, and dried cherries.
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FDA•MODERATEOphthavet Ophthalmic SolutionDechra is recalling Ophthavet Ophthalmic Solution for dogs and cats due to a lack of sterility assurance.
FDA•MODERATEAtomoxetine HCl 10mg CapsulesSafecor is recalling Atomoxetine HCl 10mg Capsules (NDC 64380-474-01) because some cartons may contain 25mg capsules due to a labeling error.
FDA•MODERATEPhilips Azurion and Allura Imaging SystemsPhilips is recalling Azurion and Allura imaging systems due to hard disk drive failure that may cause loss of functionality or data.
2 products
FDA•CRITICALMalazi 100% Pure Sudanese Sesame TahinaNassar Investment Company is recalling Malazi 100% Pure Sudanese Sesame Tahina due to potential Salmonella contamination.
FDA•MODERATEHiResolution Bionic Ear SystemAdvanced Bionics is recalling the HiRes Ultra 3D CI HiFocus Mid Scala cochlear implant due to an incorrect shelf-life expiration date.
FDA•MODERATEBD Pyxis MedStation 4000 Fingerprint ScannerCareFusion 303 is recalling the BD Pyxis MedStation 4000 medication cabinet due to a fingerprint scanner overheating burn risk.
8 products
FDA•MODERATEDuloxetine Delayed-Release Capsules 30 mgAjanta Pharma is recalling Duloxetine Delayed-Release Capsules 30 mg due to the presence of an impurity exceeding FDA recommended limits.
3 products
FDA•MODERATEErythromycin 250 mg TabletsZydus is recalling Erythromycin 250 mg tablets due to CGMP deviations and the presence of an impurity above acceptable intake limits.
2 products
FDA•CRITICALLactated Ringer's Injection USPB. Braun Medical is recalling Lactated Ringer's Injection USP due to the presence of particulate matter.
FDA•MODERATEProspector Popcorn Belgian Chocolate ToffeeProspector Popcorn Belgian Chocolate Toffee (UPC 850073852125) recalled for undeclared soy lecithin.
2 products
FDA•CRITICALMA Cohen's Kippered HerringShining Sea Fish Co. is recalling MA Cohen's Kippered Herring due to potential Clostridium botulinum contamination.
FDA•MODERATEPhilips Azurion Image-Guided Therapy SystemsPhilips is recalling various Azurion image-guided therapy systems due to mechanical wear that may impact table movement.
2 products- FDA•MODERATEPhilips Azurion X-Ray Tube Cooling Unit
Philips is recalling X-ray tube cooling units in Azurion systems due to hose degradation and potential oil leakage.
4 products 
FDA•MODERATEOasis Tears PF Lubricant Eye DropsOasis Tears PF eye drops (NDC 42126-6400-1) recalled due to lack of assurance of sterility.
FDA•MODERATEMetoprolol Succinate Extended-Release Tablets 25 mgAscend Laboratories is recalling 25 mg Metoprolol Succinate Extended-Release Tablets due to failed dissolution testing.
FDA•LOWPrimidone 50 mg TabletsGolden State Medical Supply is recalling Primidone 50 mg Tablets (NDC 51407-637-05) due to potential cross-contamination with Acemetacin.
2 products
FDA•CRITICALKroger Homestyle Cheese and Garlic CroutonsKroger Homestyle Cheese and Garlic Croutons are being recalled due to potential Salmonella contamination from an ingredient supplier.
FDA•CRITICALBD Spinal Tray with Bupivacaine HydrochlorideBecton Dickinson is recalling BD Spinal Trays (Catalog 405609) due to quality deficiencies in the included Bupivacaine Hydrochloride injection.
10 products
FDA•MODERATEPhaseOne Antimicrobial Solution SprayerOculus Technologies is recalling PhaseOne Antimicrobial Solution due to sprayer spring corrosion that may contaminate the product.
FDA•MODERATECafe Nouria Blueberry MuffinThe Brownie Baker is recalling Cafe Nouria Blueberry Muffin due to undeclared walnuts, posing a risk to those with nut allergies.
FDA•MODERATEAligned Medical Fluids KitWindstone Medical Packaging is recalling the Aligned Medical AMS16835 Fluids Kit due to a supplier recall of the included Lidocaine injection.
FDA•CRITICALGhirardelli Frozen Hot Cocoa Frappe MixGhirardelli is recalling 50 oz containers of Frozen Hot Cocoa Frappe Mix due to potential Salmonella contamination.
11 products
FDA•MODERATEAmoxicillin and Clavulanate Potassium Oral Suspension DropsCronus Pharma is recalling Amoxicillin and Clavulanate Potassium oral suspension drops for dogs and cats due to product discoloration.
2 products
FDA•MODERATEOctreotide Acetate Injectable Suspension 30 mgTeva is recalling Octreotide Acetate 30 mg injectable suspension kits (NDC 0480-9262-08) due to sterility assurance concerns from manufacturing deficiencies.
2 products
FDA•MODERATEGood & Gather Sesame Teriyaki Chicken with RiceGood & Gather Sesame Teriyaki Chicken with Rice is recalled due to undeclared sesame and soy allergens.
- FDA•LOWPrimidone 250mg Tablets
Lannett Company is recalling Primidone 250mg Tablets (NDC 0527-1231-01) due to potential cross-contamination with Acemetacin API.
FDA•CRITICALMG217 Multi-Symptom Treatment CreamWisconsin Pharmacal is recalling MG217 Multi-Symptom Treatment Cream due to Staphylococcus aureus contamination.
FDA•MODERATELiraglutide InjectionLupin is recalling Liraglutide Injection (NDC 70748-346-02 and 70748-346-03) due to white thread-like particulate matter in the cartridge.
FDA•CRITICALSolina Sourdough Cheese Crouton SeasoningSolina is recalling 50lb bags of Sourdough Cheese Crouton Seasoning due to potential Salmonella contamination.
10 products
FDA•MODERATEHydroMARK Breast Biopsy Site MarkerDevicor Medical is recalling HydroMARK breast biopsy site markers due to incorrect inner package labeling.
- Device RecallFDA•MODERATEGE HealthCare CARESCAPE Telemetry Server V5
GE HealthCare is recalling CARESCAPE Telemetry Server V5 units due to a risk of losing ECG and SpO2 monitoring capabilities.
6 products 
FDA•MODERATECASE v7.0 Cardiac Testing SystemGE Medical Systems is recalling the CASE v7.0 Cardiac Testing System due to a risk of electrical sparking and potential paper ignition.
FDA•MODERATEMedrad Avanta Injection System Tube SetsBayer is recalling Avanta Multi-Patient Administration Tube Sets due to a connection issue that may cause procedure interruptions.
FDA•MODERATEDa Vinci 5 NIR Handheld CameraIntuitive Surgical is recalling the da Vinci 5 NIR handheld camera system due to a risk of unintentional activation during surgery.
FDA•MODERATEiVIZIA Sterile Lubricant Eye DropsThea Pharma is recalling iVIZIA Sterile Lubricant Eye Drops due to a lack of assurance of sterility.
2 products
FDA•MODERATECalypso Tropic Tango LemonadeKing Juice is recalling Calypso Tropic Tango Lemonade (16 fl oz) due to undeclared Yellow No. 5.
FDA•MODERATEEnalapril Maleate Tablets, USP 20 mgRising Pharma is recalling Enalapril Maleate 20 mg tablets (NDC 64980-688-10) due to failed impurities test.
FDA•CRITICALFrench Broad Chocolate Bette's Bake Sale BonbonsFrench Broad Chocolate is recalling Bette's Bake Sale bonbons due to undeclared walnuts caused by mislabeling in the tasting guide.
FDA•MODERATEJoint Nourish Liquid SupplementWellnov Supplements is recalling Joint Nourish liquid supplement due to potential bacterial contamination and C. botulinum concerns.
14 products
FDA•MODERATEOneLIF Interbody CageNovapproach Spine is recalling 60+ variants of OneLIF Interbody Cages due to a risk of inserter attachment failure during surgery.
2 products
FDA•CRITICALPork King Good Onion & Sour Cream SeasoningPork King Good is recalling Onion & Sour Cream Seasoning due to potential Salmonella contamination in the milk powder ingredient.
FDA•MODERATESilastic Foley CathetersC.R. Bard is recalling Silastic Brand Foley Catheters due to surface staining on the devices.
FDA•MODERATECovidien Mon-a-Therm Esophageal StethoscopeCovidien is recalling Mon-a-Therm Esophageal Stethoscopes with Temperature Sensors because the devices lack FDA clearance.
3 products
FDA•MODERATEArvis Hip & Knee 3.0 Instrument Set ComponentsKico Knee Innovation is recalling Arvis Hip & Knee 3.0 instrument components over potential wear or corrosion on the magnet face.
2 products
FDA•MODERATESharpoint Microsurgical KnifeSurgical Specialties Corporation is recalling mislabeled Sharpoint microsurgical knives that contain 3.0mm blades instead of 2.2mm.
FDA•MODERATEBD PurPrep Sterile SolutionCareFusion is recalling BD PurPrep sterile solution applicators distributed nationwide due to potential contamination and sterility concerns.
2 products
FDA•CRITICALWN-976-782-1 Seasoning for Cheese SauceGivaudan Flavors Corp is recalling WN-976-782-1 Seasoning for Cheese Sauce due to an ingredient recalled by the supplier.
FDA•MODERATEBioFire Joint Infection PanelBioFire is recalling Joint Infection (JI) Panel test kits due to contamination that may lead to false positive results.
FDA•CRITICALEllsworth Sour Cream + Onion SeasoningPS Seasoning & Spices is recalling Ellsworth Sour Cream + Onion Seasoning due to potential Salmonella contamination from a supplier ingredient.
6 products