NHTSA•CRITICAL
Fontaine Fusion Flatbed Trailer Main Beams
Fontaine is recalling 2025–2026 Fusion flatbed trailers; main beams may crack due to hydrogen contamination during galvanization.
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FDA•CRITICALGeorge J Howe: 6 productsGeorge J Howe recalls sunflower seed products due to undeclared cashew allergen.
6 products
NHTSA•CRITICALGM Cadillac, Chevrolet, GMC Transfer CaseGM is recalling 2026 Cadillac, Chevrolet, and GMC 4WD/AWD vehicles and certain 2015–2020 models due to a missing transfer case component that may cause wheel lockup.
FDA•CRITICALJOHN B SANFILIPPO & SONS: 6 productsJohn B. Sanfilippo recalls nut mixes over Salmonella risk.
6 products
FDA•CRITICALUtz Quality Foods: Zapp's and Dirty Potato ChipsUtz is recalling Zapp's and Dirty potato chips in several varieties for possible Salmonella contamination.
6 products
FDA•CRITICALGriffith Foods: 3 productsGriffith Foods recalls meatloaf seasoning, milk wash, and milk-n-egg mix due to potential Salmonella.
3 products
FDA•LOWBuspirone Hydrochloride TabletsUnichem is recalling 5 mg buspirone hydrochloride tablets due to subpotency, which may reduce the medication's effectiveness.
FDA•CRITICALCook Centimeter Sizing CatheterCook recalls Centimeter Sizing Catheter (RPN N5.0-35-100-P-10S-PIG-CSC-20) over marker band cracking risk.
3 products
FDA•CRITICALIntuitive SureForm 30 Gray ReloadsIntuitive is recalling SureForm 30 Gray stapler reloads due to the risk of an incomplete staple line during surgical procedures.
FDA•LOWCVS Lidocaine Wound GelCVS is recalling Lidocaine Wound Gel (NDC 59898-950, 0.5 oz) due to failed pH specifications.
FDA•CRITICALPork King Good Onion & Sour Cream SeasoningPork King Good recalls Onion & Sour Cream Seasoning due to possible Salmonella contamination.
FDA•LOWPALAMIX uno Mixing UnitHeraeus recalls PALAMIX uno mixing units: mixing rod may loosen in units over 17 months old; shelf life reduced to 1.5 years.
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•LOWLevocarnitine Injection, USPAmerican Regent is recalling Levocarnitine Injection, USP, 1 g/5 mL single-dose vials due to missing labels.
FDA•CRITICALGhirardelli Chocolate: 11 Company CasGhirardelli recalls frappe mixes and hot cocoa over possible Salmonella contamination.
11 products
FDA•CRITICALEnoki MushroomsEnoki Mushrooms are being recalled due to potential Listeria monocytogenes contamination.
FDA•LOWMonsel's Ferric Subsulfate Solution 8 mLPremier Dental Products is recalling Monsel's Ferric Subsulfate Solution 8 mL vials (NDC 48783-112-08) due to incorrect expiration date on the vial label.
FDA•CRITICALFrench Broad Chocolate Bette's Bake Sale BonbonsFrench Broad Chocolate recalls Bette's Bake Sale bonbons over undeclared walnut allergen.
NHTSA•CRITICALREV Recreation Group Motorhome GeneratorREV is recalling 2026 Holiday Rambler motorhomes (Vacationer, Admiral, Flair, Fortis, Bounder) due to furnace-triggered unexpected generator operation risking carbon monoxide poisoning.
FDA•LOWMagnesium Chloride 6-Hydrate Crystal 500GAvantor is recalling Magnesium Chloride 6-Hydrate Crystal 500G bottles (NDC 10106-2448-1) due to subpotency.
NHTSA•CRITICALWinnebago Ekko Motorhome TouchscreenWinnebago Ekko motorhomes (2022–2027) may have phantom touchscreen inputs that turn on the generator, risking carbon monoxide poisoning in enclosed spaces.
FDA•CRITICALMedline Namic Angiographic Control SyringesWindstone recalls kits with Medline Namic RA Syringes over risk of adapter unwinding, which may cause disconnection and serious injury.
FSIS•CRITICALAjinomoto Fried Rice, Ramen, and Shu MaiThe recall includes a wide range of ready-to-eat and not-ready-to-eat items sold nationwide.
3 products
NHTSA•CRITICAL2026 Nissan Frontier Pro4X R Steering ComponentsRoush is recalling 2026 Nissan Frontier Pro4X R vehicles over loose or missing steering fasteners that may cause loss of control.
FDA•CRITICALB. Braun STREAMLINE Bloodline SetB. Braun recalls STREAMLINE bloodline sets for Dialog DR over arterial line air bubble risk.
6 products
FDA•LOWIsland Kinetics: multiple gelsIsland Kinetics recalls hydrocortisone 1% gels (Remedy Gel, Skin Rehab, Essential Calming) due to subpotency.
3 products
FDA•CRITICALBlaine Labs: multiple drugsBlaine Labs recalls multiple topical antiseptic/antifungal gels and creams due to Lysinibacillus fusiformis contamination.
9 products
FDA•CRITICALMedline Convenience Kits with Namic RA SyringesMedline recalls convenience kits with Namic RA syringes over risk of loose connection or disconnection during use.
25 products
FDA•CRITICALWawa Beverage: 4 productsWawa recalls 16 oz Iced Tea Lemon, Diet Iced Tea Lemon, Diet Lemonade, and Fruit Punch over undeclared milk allergen.
4 products
NHTSA•CRITICALIS300 Slave Cylinder Conversion Kit Adapter PlateSleepy Customs is recalling IS300 Slave Cylinder Conversion Kits; adapter plate may separate, causing loss of clutch and gear-shift function.
FDA•CRITICALRaw Farm: 5 productsRaw Farm recalls raw cheddar cheeses over possible E. coli O157:H7 outbreak.
5 products- Device RecallFDA•CRITICALPhilips Respironics Trilogy Evo O2 Ventilator
Philips Respironics recalls Trilogy Evo O2 ventilators (SW 1.05.15.00) over delayed obstruction alarm.
4 products 
FDA•LOWSuper World Trading: 3 Heshan Mei Heong Yuen Food Pte NiesMei Heong Yuen roasted peanuts recalled over banned cyclamate sweetener.
3 products
FDA•CRITICALCentrosFLO Hemodialysis CathetersMerit Medical recalls CentrosFLO Hemodialysis Catheters over sheath introducer defect that may cause hemorrhage and other serious complications.
5 products
NHTSA•CRITICALYamaha TW200 SpeedometerYamaha is recalling 2026 TW200 motorcycles with speedometer failure that may increase crash risk.
- Device RecallFDA•CRITICALPhilips Respironics Trilogy Evo Ventilator
Philips Respironics recalls Trilogy Evo ventilators over tidal volume discrepancy with non-pneumatic nebulizers.
4 products 
NHTSA•CRITICALNissan LEAF High Voltage Battery ModuleNissan is recalling 2026 LEAF vehicles over high voltage battery short-circuit fire risk.
FDA•CRITICALMagnesium Sulfate in Water for Injection IV BagsAmneal recalls Magnesium Sulfate IV bags due to product mix-up with Tranexamic Acid.
FDA•CRITICALHandy Solutions Neck & Shoulders Heating PadHandy Solutions Neck & Shoulders Heating Pad (Model 25607) may overheat and cause burns if folded or placed under the body.
FDA•LOWSodium Iodide I-131 Kit Gelatin Capsule PackRadnostix is recalling Sodium Iodide I-131 Kit capsule packs due to failed product specifications.
FDA•CRITICALErbe Flexible CryoprobeErbe USA recalls Flexible Cryoprobes because probes may rupture or burst during use.
4 products
FDA•LOWDatascope Cardiosave Battery Charging StationDatascope is recalling the Cardiosave battery charging station due to a screw defect in the left bay that prevents proper charging.
FDA•CRITICALWebcol Alcohol Prep Pads (70% Isopropyl Alcohol)Cardinal Health is recalling Webcol Alcohol Prep Pads (200-count boxes) due to microbial contamination that may pose infection risk.
3 products
FDA•CRITICALBluegrass Ingredients: Butter-Rich Powder and Butter PowderBluegrass Ingredients recalls Butter-Rich and Butter Powder (50 lb.) over Salmonella risk.
2 products
FDA•CRITICALOmnipod 5 PodsInsulet is recalling Omnipod 5 Pods due to a cannula defect that can cause insulin under-delivery and severe health risks.
NHTSA•CRITICALVision Wheel Aftermarket Aluminum WheelsVision Wheel is recalling aftermarket aluminum wheels (part numbers 640-6744GBMF38, 640-6765GBMF40, 640-7710GBMF40, 640-7744GBMF40, 640-7765GBMF40) that may crack and cause loss of vehicle control.
2 products
NHTSA•CRITICALEscape Trailer Recreational Trailer Spare Tire CarrierEscape Trailer recalls 2025 E17, E19, E21, E5.0 trailers; spare tire carrier may detach due to welding defect.
FDA•LOWCipla: Multiple Packaged In Cartons CapsulesCipla recalls Nilotinib 150 mg and 200 mg capsules over failed specification tests.
2 products
FDA•CRITICALImpella RP Flex with SmartAssistAbiomed recalls Impella RP Flex with SmartAssist due to sensor drift risk.
3 products
FDA•LOWEptifibatide Injection 75 mg/100 mLSlate Run Pharmaceuticals recalls Eptifibatide Injection 75 mg/100 mL vials (NDC 70436-027-80, 70436-163-80) due to incorrect dosing-route labeling.