FDA•MODERATE
PReye Vitamin See Antioxidant Eye Drops
PReye is recalling Vitamin See Antioxidant Preservative Free Eye Drops due to a lack of assurance of sterility.
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FDA•MODERATEOctopus Evolution Tissue StabilizerMedtronic recalls Octopus Evolution Tissue Stabilizer TS2000 due to incorrect tubing assembly.
3 products
FDA•MODERATESurgify Halo BurrSurgify Halo 3.0 mm burr recalled due to potential breakage during spinal surgery.
19 products
FDA•MODERATEStryker InZone Detachment SystemStryker is recalling the InZone Detachment System due to premature battery drain that may prevent coil detachment during medical procedures.
FDA•MODERATEDuloxetine Delayed-Release CapsulesDirect Rx is recalling 30 mg Duloxetine Delayed-Release capsules due to N-nitroso-duloxetine impurity levels exceeding FDA limits.
FDA•MODERATEAcumed Hexalobe ScrewsAcumed is recalling various hexalobe screws used in wrist fixation systems due to a risk of the screws breaking during use.
2 products
FDA•MODERATEAmgen Corlanor and Sensipar TabletsAmgen recalls Corlanor and Sensipar tablets over foreign substance contamination.
5 products
FDA•MODERATEZimmer Off-Axis Reamer GuideZimmer recalls Off-Axis Reamer Guide (Model 110040240) due to breakage risk from catching during reaming.
5 products
FDA•MODERATEJoy Gourmet Foods: 14 productsJoy Gourmet recalls Joy brand lassi drinks over inadequate pasteurization.
14 products
FDA•MODERATEPFM Medical Multi-Snare SetPFM Medical is recalling Multi-Snare Set catheter devices due to a failure to meet biocompatibility requirements for in-vitro cytotoxicity.
FDA•MODERATEVentec VOCSN+Pro Respiratory SystemVentec is recalling the VOCSN+Pro respiratory system because a damaged battery may prevent the backup alarm from sounding during power loss.
FDA•MODERATEMethylergonovine Maleate TabletsMajor Pharmaceuticals is recalling 0.2 mg Methylergonovine Maleate Tablets due to subpotency.
FDA•CRITICALMidwest Legacy Raw Beef Dog FoodMidwest Legacy is recalling Raw Beef Dog Food over potential Salmonella, Listeria, and E. coli contamination.
FDA•MODERATEFenofibrate Capsules, USP 200 mgAjanta Pharma is recalling Fenofibrate Capsules, USP 200 mg, due to manufacturing process deviations.
FDA•MODERATEPhilips Avalon Fetal Monitor FM20Philips recalls Avalon Fetal Monitor FM20 over speaker connector issue that may cause loss of speaker output.
2 products
FDA•MODERATEBoichik Bagels: 3 productsBoichik Bagels recalls Whitefish Salad, Tuna Salad, and Pumpernickel Mix Bagels over undeclared eggs.
3 products
FDA•MODERATEDa Vinci Surgical System E-Brake Retainer PinIntuitive Surgical is recalling the Da Vinci surgical system E-brake retainer pin due to a risk of uncontrolled motion and patient injury.
FDA•MODERATETMJ Bilateral ImplantsTMJ Solutions is recalling custom temporomandibular joint implants due to incorrect components causing a poor fit and potential open bite.
FDA•MODERATEMorningstar Farms: 2 productsMorningStar Farms recalls Buffalo Chik'n Nuggets and Hot & Spicy Sausage Patties over possible plastic contamination.
2 products
CPSC•Arizer Solo III Portable VaporizersArizer is recalling Solo III portable vaporizers due to fire and burn hazards affecting specific serial prefixes and UPC 628078802274.
CPSC•BABESIDE Doll and Stroller Toy SetsBABESIDE doll and stroller sets are recalled due to a choking hazard from small parts that violate federal safety standards.
CPSC•Pyro Diablo Diablo Rising FireworksPyro Diablo "Diablo Rising" fireworks (model PD-C5001) are recalled due to explosion and burn hazards from excessive pyrotechnic composition.
CPSC•GOPO Toys Pull String Teething ToysGOPO Toys is recalling pull string teething toys due to a serious choking hazard caused by strings that violate federal safety standards.
CPSC•Joolz Aer2 Car Seat AdaptersJoolz is recalling Aer2 car seat adapters because they can fail to attach to the stroller, posing a fall hazard to children.
CPSC•CooCooBaby Baby LoungersCooCooBaby is recalling Classic and Deluxe baby loungers due to suffocation and fall hazards that violate federal infant sleep safety standards.
CPSC•Michley Children's PajamasMichley children's pajamas are recalled for failing to meet federal flammability standards, posing a serious burn injury or death risk.
CPSC•Veseacky Children's Pajama SetsVeseacky children's pajama sets are recalled for violating federal safety standards, posing a serious burn injury or death risk to children.
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.
CPSC•Arrogantf Spa Drain CoversArrogantf spa drain covers are recalled due to entrapment and drowning hazards, as they violate federal safety standards.
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.