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Evergreen Fresh Sprouts Broccoli Sprouts
Broccoli Sprouts recalled over possible Salmonella contamination.
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FDA•0.9% Sodium Chloride Injection, USP, 100 mL Partial FillB. Braun recalls 0.9% Sodium Chloride Injection, 100 mL Partial Fill, due to particulate matter (iron oxide, cellulose, polystyrene).
FDA•MODERATEAMS DSAEK Pack Convenience KitWindstone recalls AMS DSAEK Pack kits (Part AMS12394B) due to detached blue BOPs in saline bags.
FDA•MODERATEMedicaLyte Liquid Bicarbonate ConcentrateNipro recalls MedicaLyte hemodialysis concentrate (REF BC-100, BC+201) over high endotoxin levels.
4 products
FDA•fentaNYL Citrate Injection 1,000 mcg/100 mLOurPharma recalls fentaNYL Citrate Injection 1,000 mcg/100 mL over mislabeled expiry dates; NDC 73013-1013-01.
FDA•Alfalfa 50 lb BagsAlfalfa 50 lb bags recalled over potential E. coli and Salmonella contamination.
- Food RecallFDA•MODERATEFannie May & XO Marshmallow Pixie S'mores Collection
Fannie May & XO Marshmallow Pixie S'mores Collection recalled for undeclared milk and pecans.
FDA•CRITICALEpidural/Pain TQC KitMedical Action recalls its Epidural/Pain TQC Kit containing sodium chloride ampules over compromised sterility.
2 products
FDA•BMC Luna G3 APAP (LG3600)BMC recalls Luna G3 APAP devices with faulty firmware G3-2.00.76; check your device's firmware.
FDA•Fi Dog SupplementsFi recalls dog supplements over Salmonella risk
FDA•Cranberry Chicken Salad Wedge SandwichFreshPoint recalls Cranberry Chicken Salad Wedge Sandwiches over undeclared egg allergen.
FDA•LOWPovidone Iodine/Proparacaine Ophthalmic SolutionImprimis NJOF recalls ophthalmic solution for being subpotent, risking reduced efficacy.
FDA•LOWFluphenazine HCl Tablets 1mgAjanta Pharma recalls Fluphenazine HCl 1mg tablets (NDC 27241-255-01) due to impurity out-of-specification.
FDA•Made Fresh Salads Deli Style Salads and Cream CheeseMade Fresh Salads is recalling Ready to Eat Deli Style Salads and cream cheese over potential Listeria contamination.
FDA•Foods Alive Organic Moringa Leaf PowderFoods Alive recalls 8 oz organic moringa leaf powder over possible Salmonella contamination.
FDA•Business Pill and Branch Manager for MenSUPPLX.com recalls Business Pill and Branch Manager for Men supplements due to undeclared yohimbine.
FDA•CRITICALCrown Farms Dried Suri CutEuro Foods recalls Crown Farms Dried Suri Cut (200 gm) over improper evisceration.
FDA•MODERATESoft PVC Thoracic CathetersThis recall involves thoracic catheters manufactured for use in draining fluid or air from the chest cavity.
3 products
FDA•MODERATEDermaV Laser SystemLutronic recalls DermaV Laser System over burn risk from spark/loud noise at high fluences.
FDA•MODERATEHeartSine Samaritan PadsSee the official recall notice for details about this display summary.
FDA•MODERATEHalyard IV Start KitAVID Medical recalls Halyard IV Start Kits (REF KRIV26-02) due to sterility concerns with included applicators.
FDA•Epinephrine Injection 30 mg/30 mLAmerican Regent recalls epinephrine 30 mg/30 mL vials due to glass particulates and sterility concerns.
FDA•Great Value Organic Triple Berry BlendGreat Value Organic Triple Berry Blend 10 OZ recalled due to potential E. coli O145 contamination.
FDA•LOWTrokendi XR (topiramate) Extended-Release CapsulesTrokendi XR (topiramate) 50 mg capsules recalled over failed dissolution specs.
FDA•MODERATEMycophenolate Mofetil for InjectionMylan recalls Mycophenolate Mofetil for injection, 500 mg/vial, over failed dissolution specs.
FDA•MODERATEBD Urinary Catheter Trays with CliniClean Pericare WipesBD Urinary Catheter Trays with CliniClean Pericare Wipes recalled over possible lubricant contamination causing skin irritation.
12 products
FDA•MODERATEGRANUFLO Dry Acid ConcentrateFresenius recalls GRANUFLO Dry Acid Concentrate (0FD2251-3B, 0FD3251-3B) over blue-green discoloration.
3 products
FDA•MODERATEtraZODone Hydrochloride Tablets, USP, 50 mgTeva recalls traZODone HCl 50 mg tablets due to foreign tablets/capsules in product.
FDA•MODERATEFresenius 5008X Blood Tubing SetFresenius recalls 5008X blood tubing set (PN 03-5110-6) over blood leak risk.
4 products
FDA•MODERATEDiscofix Four Way StopcockB Braun recalls Discofix Stopcock Sets over incorrect expiration date on carton label.
- Device RecallFDA•MODERATELUX-Dx Insertable Cardiac Monitor System Software
Boston Scientific recalls LUX-Dx ICM server software (Model 7260) over delayed AF Burden Alerts.
3 products 
FDA•LOWWonton Specialists: 6 productsWonton Specialist recalls noodles and dumpling skins for undeclared FD&C Red No. 40, an allergen risk.
6 products
FDA•MODERATEVelys Enabling Tech Robotic-Assist StationMedos recalls Velys Robotic-Assist Station over software issue causing unintended arm movement.
FDA•MODERATEPooled Cryoprecipitated AHFVitalant recalls Pooled Cryoprecipitated AHF for not meeting specifications.
FDA•CRITICALAddall XR ShotAddall XR Shot recalled for undeclared 1,4-DMAA, Phenylethylamine, and Phenibut.
- Device RecallFDA•MODERATEPhilips Brilliance CT Systems
Philips recalls Brilliance iCT and related CT systems over unintended radiation issue.
4 products 
FDA•MODERATELexia: Multiple Broadway Joe's Pain CreamsLexia LLC recalls Broadway Joe's Pain Cream over potential raw material contamination.
2 products
FDA•2% Chlorhexidine Gluconate ClothsSage Products recalls 2% Chlorhexidine Gluconate Cloths over possible cross-contamination.
FDA•Lipofit Extreme 2.0 Fat BurnerLipofit Extreme 2.0 Fat Burner recalled over undeclared fluoxetine and toxic DNP.
FDA•Kofinas Garlic Mediterranean Infused Extra Virgin Olive OilKofinas recalls Garlic Mediterranean Infused Extra Virgin Olive Oil (500/250/100 ml) due to unapproved garlic essential oil.
FDA•Crystal Temptations Chocolatey EyeballsCrystal Temptations recalls Chocolatey Eyeballs due to undeclared milk allergen.
FDA•Buprenorphine Sublingual Tablets 2 mgAmerican Health Packaging recalls Buprenorphine Sublingual Tablets 2 mg over a label mix-up.
FDA•MODERATEMedline Convenience Kits with BD ChloraPrep Clear 1mL ApplicatorsMedline recalls Convenience Kits with BD ChloraPrep Clear 1mL Applicators over possible open or incomplete seals.
13 products
FDA•MODERATEBaxter Novum IQ Syringe PumpBaxter recalls Novum IQ Syringe Pump over a software issue during multi-syringe infusions.
2 products
FDA•MODERATEHEALON EndoCoat PRO and DUET PRO IIJ&J Surgical Vision updates instructions for HEALON viscoelastic products used in cataract surgery over cannula insertion risks.
FDA•MODERATEApheresis Platelets, Leukocytes Reduced, IrradiatedNew York Blood Center Enterprises recalls Apheresis Platelets, Leukocytes Reduced, Irradiated units over excessive platelet count.
FDA•LOWApheresis Red Blood Cells, Leukocytes Reduced, IrradiatedNew York Blood Center recalls apheresis red blood cells over incorrect anticoagulant ratio.
FDA•MODERATEMedline Convenience KitsMedline recalls two convenience kits over sterility breach risk in included BD ChloraPrep and FREPP applicators.
16 products
FDA•Morasch Meats: 2 Raw Frozen Net Weight PackagedsNorthwest Naturals raw cat and dog diets recalled over Salmonella risk.
2 products
FDA•Martina MangoesPanorama Produce recalls Martina mangoes over possible Salmonella contamination.