FDA•MODERATE
Morningstar Farms: 2 products
MorningStar Farms recalls Buffalo Chik'n Nuggets and Hot & Spicy Sausage Patties over possible plastic contamination.
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FDA•Clover Hill Dairy CheeseClover Hill Dairy expands recall of all brand cheeses due to possible Listeria contamination.
FSIS•MODERATEPower Plate Meals Meatloaf with Garlic Mashed PotatoesPower Plate Meals recalls 5,795 lbs of frozen meatloaf with garlic mashed potatoes due to undeclared soy allergen.
FDA•MODERATEKeystone Industries: Multiple Topical Anesthetic GelsKeystone recalls 20% benzocaine gels (Pearson, Quala, DHP, etc.) over defective seals.
7 products
FDA•MODERATECold Brew Coffee ConcentrateFairhope Roasting recalls Cold Brew Concentrate; missing 'Keep Refrigerated' label on 1-gallon jugs.
FDA•CRITICALGiraffe Stand-alone Infant Resuscitation SystemDatex-Ohmeda recalls Giraffe infant resuscitation systems over oxygen concentration risk.
3 products- Device RecallFDA•MODERATEHeartMate 3 LVAS Backup Battery
Thoratec recalls HeartMate 3 LVAS kits (model 106524US) due to 11V backup battery failures.
6 products 
FDA•MODERATEInternational Food Products: 3 productsInternational Food Products recalls dressing stabilizer and dairy powders over possible Salmonella.
3 products
FDA•LOWUnited Salt Corp SaltUnited Salt Corp recalls mislabeled salt: plain vs. iodized mix-up.
FDA•MODERATEInspire Respiratory Sensing LeadInspire is recalling its Respiratory Sensing Lead (Model 4340) due to incorrect Use By Dates that may lead to premature revision surgery.
3 products
FDA•MODERATEAdndale Magnesium Glycinate GummiesAdndale Magnesium Glycinate Gummies are being recalled due to the presence of undeclared melatonin.
FDA•CRITICALImpella CP Set with SmartAssistAbiomed is recalling Impella CP Sets with SmartAssist due to a risk of low purge pressure that may interrupt mechanical circulatory support.
FDA•MODERATEBD Connecta Luer-Lok StopcockBD is recalling Connecta Luer-Lok stopcocks due to a potential connection failure at Port C when using plastic luer-lok syringes.
FDA•MODERATESplashwire Hydrophilic Guide WireMerit Medical is recalling various Splashwire Hydrophilic Guide Wire models due to unsealed pouches that may compromise device sterility.
2 products
FDA•MODERATEBuprenorphine HCl InjectionPar Health is recalling Buprenorphine HCl Injection due to crystallization identified as Buprenorphine free base.
FDA•MODERATETriathlon Universal Baseplate Size 3/4Stryker recalls Triathlon Universal Baseplates due to size mislabeling in packaging.
2 products
FDA•MODERATEMedline Red Rubber Latex Urethral CathetersMedline recalls Red Rubber Latex Urethral Catheters (REF DYND13508–DYND13522, DYND13614/16) over surface, connector, and diameter defects.
34 products
FDA•MODERATEGiraffe OmniBed Canopy SoffitGE HealthCare recalls Giraffe OmniBed incubator/warmer over canopy soffit fastener risk that could injure patients.
3 products
FDA•MODERATEConMed AirSeal 5 mm Access PortConMed recalls AirSeal 5 mm Access Port (iASB5-150) over overpressure alert risk.
11 products- Device RecallFDA•MODERATESTAAR ICL Calculation Software
Staar Surgical is recalling Version 8.00 of its ICL Calculation Software due to a coding error affecting toric lens orientation diagrams.
2 products 
FDA•CRITICALTaro CakesE & S Grocery & Bakery is recalling Taro Cakes due to an undeclared egg allergen.
FDA•MODERATEPhilips MultiDiagnost Eleva Hand SwitchPhilips recalls MultiDiagnost Eleva systems over hand switch that may not release, risking unintended radiation.
3 products
FDA•MODERATENutrisystem Chocolate CheesecakeNutrisystem is recalling Chocolate Cheesecake 2 oz packages due to an undeclared soy allergen.
FDA•CRITICALAl Yaman Halawa Extra PistachioAl Yaman Halawa Extra Pistachio 907g jars recalled over possible Salmonella contamination.
FDA•MODERATEGreat Value Hawaiian Roll 4pkGreat Value Hawaiian Roll 4pk recalled over oily substance on food-contact packaging; product never reached store shelves.
FDA•MODERATERitmed Neurological SpongesAMD Medicom recalls Ritmed Neurological Sponges due to elevated endotoxin risk; full REF list on FDA page.
2 products
FDA•MODERATEdirectCHECK ACT-LR Whole Blood Quality ControlAccriva Diagnostics is recalling directCHECK ACT-LR whole blood quality control, level 2, due to incorrect performance range labeling.
FDA•MODERATEMID DOLCIARIA SRL: 2 Via Casalini BelpassosMID DOLCIARIA recalls Cannoli Siciliani and Crunchy Cannoli Gluten Free over unapproved colors E140/E141.
2 products
FDA•MODERATETrigen Proximal Straight Humeral NailSmith & Nephew is recalling the Trigen Proximal Straight Humeral Nail due to a manufacturing error that may cause surgical delays or revision.
FDA•CRITICALFirst Street Dark Chocolate RaisinsFirst Street Dark Chocolate Raisins are recalled due to undeclared peanuts, which pose a risk to consumers with peanut allergies.
FDA•MODERATEAripiprazole 30 mg TabletsAjanta Pharma is recalling Aripiprazole 30 mg tablets due to a mix-up with Voriconazole 50 mg tablets.
FDA•MODERATEMedtronic O-arm O2 Imaging SystemMedtronic is recalling the O-arm O2 Imaging System due to a firmware anomaly that may cause image artifacts during clinical use.
FDA•MODERATEHarmonyAIR A-Series Surgical Lighting SystemHarmonyAIR A-Series surgical lights recalled: intensity buttons may detach.
2 products
FDA•MODERATEHarmonyAIR A-Series Surgical Lighting SystemSteris is recalling HarmonyAIR A-Series Surgical Lighting Systems due to a risk of paint delamination on the light heads.
FDA•CRITICALNara Organics Whole Milk Organic Infant FormulaNara Organics is recalling Whole Milk Organic Infant Formula over potential Clostridium botulinum contamination.
FDA•MODERATEPepperoni Rolls 5 ozPepperoni Rolls recalled for undeclared milk allergen and improper refrigeration; 5 oz packages.
FDA•MODERATEDabur India: Multiple Made In India ProductsDabur India recalls 14 OTC topical products over CGMP deviations.
14 products
FDA•MODERATEChlorthalidone 25 mg TabletsChlorthalidone 25 mg tablets are being recalled due to failed dissolution specifications.
FDA•LOWFocalin XR 5 mg CapsulesSandoz is recalling Focalin XR 5 mg capsules due to missing or incorrect lot numbers and expiration dates on the product labels.
FDA•MODERATEAlyacen 7/7/7 TabletsGlenmark is recalling Alyacen 7/7/7 tablets due to out-of-specification results for total impurities.
FDA•MODERATEVasopressin 2 Units/2 mL SyringesIntegraDose is recalling Vasopressin 2 Units/2 mL syringes due to subpotency, which may cause the drug to be ineffective.
FDA•MODERATEPAI: Multiple Kerr Insta-char In An ProductsVistaPharm recalls Kerr Insta-Char activated charcoal (25g/50g) for failing OTC monograph requirements.
4 products
FDA•MODERATEMedline EBSI KitMedline recalls EBSI Kit (EBSI1534) due to cracked butyrate tubing and recalled MASTISOL adhesive.
42 products
FDA•CRITICALImpella Heart Pump Software RecallAbbott's Impella heart pumps may fail to restart after certain operational faults, posing a serious health risk to patients.
2 products
FDA•CRITICALParacentesis KitArrow International recalls paracentesis kits due to supplier quality issues with included injectables, risking serious injury.
51 products
FDA•CRITICALAzuma Foods Tako Wasabi Seasoned OctopusAzuma Foods is recalling Tako Wasabi Seasoned Octopus due to undeclared fish.
FDA•MODERATENiacin Extended-Release Tablets 1,000 mgGolden State Medical Supply is recalling Niacin Extended-Release Tablets, 1,000 mg, due to failure to meet dissolution specifications.
2 products
FDA•MODERATEFresh Roast Systems ColorTrack InstrumentFresh Roast Systems is recalling the ColorTrack instrument (Model BENCH R-100) due to a potential laser safety hazard.
FDA•MODERATEHalyard Pain PackAVID Medical recalls Halyard Pain Pack kits (AMPK48-01) over possible lack of sterilization.
4 products
FDA•MODERATEMOSAIQ Oncology Information SystemElekta is recalling the MOSAIQ Oncology Information System due to a software error that may prevent the loading of baseline shift plans.