FDA•MODERATE
Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset
Pure Solutions recalling 1 fl oz sleep formula bottles due to undeclared milk allergen from bovine colostrum.
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FDA•MODERATECoco's Italian Market Cannoli Making KitCoco's Italian Market is recalling Cannoli Making Kits due to undeclared wheat and milk allergens.
2 products
FDA•CRITICALPrime Food Processing Dried Croaker FishPrime Food Processing is recalling Dried Croaker Fish due to the risk of botulism from uneviscerated fish.
FDA•MODERATEEquinoxe Ergo Modular Impactor HandleExactech is recalling the Equinoxe Ergo Modular Impactor Handle due to a missing cross-pin that may cause device failure.
2 products
FDA•MODERATEImactis CT-Navigation SystemGE Medical Systems is recalling Imactis CT-Navigation System (Models E85101LA, E85101LP) due to potential needle trajectory/tip position discordance.
FDA•MODERATEIBA Proton Therapy System PROTEUS 235IBA PROTEUS 235 proton therapy systems may fail to stop beam delivery if external gating device signal is lost, risking patient mistreatment.
FDA•MODERATEPro Numb Tattoo Numbing SprayPro Numb is recalling 5% Lidocaine Tattoo Numbing Spray due to cGMP manufacturing deviations.
2 products
FDA•MODERATEB. Braun Winged Infusion SetsB. Braun is recalling 21GA Winged Infusion Sets (Model 7M2802) due to potential needle tip dullness or breakage.
3 products
FDA•MODERATEMICS3 Angled Sagittal Saw AttachmentHowmedica Osteonics is recalling MICS3 Angled Sagittal Saw Attachments because external screws may loosen and detach during use.
FDA•MODERATEOn-X Mitral Heart Valve with Conform-X Sewing RingOn-X is recalling Model ONXMC-25/33 Mitral Heart Valve due to incomplete testing before distribution.
FDA•CRITICALKirkland Signature Mini BeignetsKirkland Signature Mini Beignets are recalled due to undeclared hazelnut, posing a risk to those with hazelnut allergies.
FDA•CRITICALMolly Kitchen's Tuna SaladReser's Fine Foods is recalling Molly Kitchen's Tuna Salad due to undeclared fish allergen from incorrect lid labeling.
2 products
FDA•CRITICALKarns Foods Mini Dark Chocolate Raspberry CupsKarns Foods is recalling 8 oz Mini Dark Chocolate Raspberry Cups due to undeclared peanuts.
FDA•MODERATETiki Bar Dark Chocolatey Peanut Butter & PretzelTiki Bar Dark Chocolatey Peanut Butter & Pretzel is recalled due to an undeclared peanut allergen.
FDA•MODERATEBeckman Coulter Chemistry AnalyzersBeckman Coulter is recalling chemistry analyzers due to a software error that may cause system delays and impact patient diagnosis.
2 products
FDA•MODERATEMedline Cardiac Procedure KitsMedline is recalling cardiac procedure kits to clarify that the included chest drainage units are intended for adult patients only.
FDA•MODERATEMiniMed 780G Insulin PumpMedtronic is recalling MiniMed 780G insulin pumps (models MMT-1884, MMT-1886) running software 6.60-6.62 due to insulin delivery inaccuracies.
- Device RecallFDA•MODERATECentricity Universal Viewer Software
GE is recalling Centricity Universal Viewer software versions 5.0 and 7.0 due to a cybersecurity vulnerability that may expose user credentials.
4 products - Device RecallFDA•MODERATEHealthCast Vital Sync Remote Patient Monitoring System
Covidien is recalling Vital Sync software because patient bedside monitor alarms may fail to transmit to the remote monitoring system.
2 products 
FDA•MODERATETandem Insulin Infusion PumpTandem is recalling insulin infusion pumps in Czech Republic and Slovakia due to user guide translation errors that could cause unintended insulin delivery.
CPSC•Primark The Nightmare Before Christmas Glow-in-the-Dark Coloring SetPrimark is recalling The Nightmare Before Christmas Glow-in-the-Dark Coloring Sets (code 0309401) due to high strontium and aluminum levels in crayons, posing a poisoning hazard to young children.
CPSC•Sunneday and Blue Bay Above-Ground PoolsStarmatrix Group recalls Sunneday and Blue Bay above-ground pools (models 70018, 70024, 358015W, 359015G, 360018W, 361018G, 380018T) over drowning hazard from compression strap footholds.
CPSC•NorthStar Hot Water Pressure WashersNorthStar is recalling three pressure washer models (items 157310, 157594, 157595) made Jan–Aug 2025 due to fan wheel failure risk causing flames and smoke.
CPSC•Urban Arrow FamilyNext Pro Cargo E-BikeGazelle USA recalls Urban Arrow FamilyNext Pro Cargo E-Bikes with defective Fidlock buckles that may fail to latch with children in cargo area.
CPSC•LuxJet Submersible LED LightsLuxJet Submersible LED Lights with accessible lithium coin batteries pose serious ingestion hazard to children; can cause internal burns and death.
CPSC•Bazic Silicone Glue Model 2030Bazic is recalling Silicone Glue Model 2030 (batch V01233-031725-70004523) over non-child-resistant packaging of methanol-containing product and incorrect labeling.
CPSC•Hobby Lobby Giraffe and Llama Plush Toys with ClipsHobby Lobby recalls Giraffe and Llama plush toys (models HL699436/HL731481) due to detachable legs releasing small beads—choking hazard.
CPSC•AiTuiTui Pull String Teething ToyAiTuiTui Pull String Teething Toy (Model 688-59) recalled for choking hazard; violates toy safety standards.
CPSC•Mindbodygreen Ultimate Multivitamin+ Dietary SupplementMindbodygreen recalls Ultimate Multivitamin+ bottles (UPC 850027975177, 850027975429) over non-child-resistant packaging containing iron.
CPSC•Trek and Electra Electric Bicycle Rear Wheel BoltsHyena is recalling rear wheel bolts on 2026 Trek FX+ and Electra Townie Go! e-bikes sold before October 2025 due to fall hazard from wheel separation.
CPSC•Viofairy Hair Growth Serum BottlesViofairy Hair Growth Serum (5% minoxidil) recalled for non-child-resistant packaging; risk of serious injury or death if swallowed by children.
CPSC•Sefudun 5% Minoxidil Hair Growth Serum KitSefudun 5% Minoxidil Hair Growth Serum Kit lacks child-resistant packaging, risking serious injury or death if ingested by children.
FDA•MODERATEPreema Bright Red and Orange Food Colour PowderPreema Bright Red and Orange Food Colour Powder recalled for banned carmoisine and undeclared FD&C Yellow 5 and Red 40.
2 products
FDA•MODERATEMetoprolol Succinate Extended-Release TabletsTeva is recalling Metoprolol Succinate Extended-Release Tablets due to failed dissolution specifications.
4 products
FDA•MODERATEOlympus Single Use Biopsy ValveOlympus is recalling the MAJ-210 single use biopsy valve due to the risk of rubber fragments detaching during use.
2 products
FDA•MODERATEParadise Ultrasound Renal Denervation CatheterReCor Medical is recalling the Paradise Ultrasound Renal Denervation Catheter (Model PRDS-068-02) as these units were not for human use.
3 products- Device RecallFDA•MODERATEB. Braun Cesk Northside Anesthesia Tray
B. Braun is recalling the Cesk Northside Anesthesia Tray (Model 555076) due to potential cracking of the included adhesive tubing.
8 products 
FDA•CRITICALFrozen Fish BallsFrozen Fish Balls are being recalled due to undeclared wheat and sesame allergens.
3 products
FDA•CRITICALWhy Not Natural Moringa CapsulesWhy Not Natural is recalling Moringa Capsules due to potential Salmonella contamination.
FDA•MODERATEJiffy Original Composite Polisher Cups (Coarse)Ultradent is recalling Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011, due to crumbling and breakage risk.
FDA•MODERATEMedline Medcrest Surgical GownsMedline is recalling Medcrest surgical gowns due to a risk of fabric delamination during laundering, which may lead to infection.
3 products
FDA•CRITICALHycoat Hyaluronate Sodium Sterile SolutionNeogen is recalling Hycoat Hyaluronate Sodium Sterile Solution for veterinary use due to potential microbial contamination.
2 products
FDA•MODERATEFrozen Half Shell OystersKhee Trading is recalling frozen half shell oysters due to potential Norovirus contamination.
FDA•MODERATEDiclofenac Sodium Topical Gel 3%Taro Pharmaceuticals is recalling Diclofenac Sodium Topical Gel 3% (100 g) due to viscosity specification failure.
FDA•CRITICALImpella RP Flex with SmartAssistAbiomed is recalling Impella RP Flex with SmartAssist devices due to a potential malfunction of the differential pressure sensor.
3 products
FDA•MODERATEBD 10mL Non-Sterile Luer-Lok SyringeBD is recalling 10mL non-sterile Luer-Lok syringes (catalog 301029) due to incorrect Luer Slip syringes mixed into batches.
FDA•MODERATELutronic CLARITY II Laser SystemLutronic is recalling CLARITY II Laser System (Model 1110200210) due to sparking and burn hazard.
FDA•MODERATEKeto-C Antiseptic WipesStratford Care USA is recalling Keto-C Antiseptic Wipes (50ct) due to misbranding; product contains non-medicated otic flush instead of labeled antiseptic.
36 products
FDA•MODERATERepackaged M&Ms Peanut CandiesBeacon Promotions is recalling 1.3 oz repackaged M&Ms Peanut candies due to undeclared milk, soy, and peanut allergens.
3 products
FDA•MODERATEGerber Arrowroot BiscuitsGerber Arrowroot Biscuits (5.5 oz, UPC 015000005962) recalled for potential paper/plastic contamination in arrowroot flour.