FDA•CRITICAL
PS Seasoning & Spices: 6 products
PS Seasoning & Spices recalls Ellsworth Sour Cream + Onion Seasoning and five other products over possible Salmonella from recalled milk powder.
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FDA•LOWPrimidone Tablets 250 mgAmerican Health Packaging recalls Primidone 250 mg tablets over API cross contamination.
2 products
FDA•LOWBusulfan InjectionSagent Pharmaceuticals is recalling Busulfan Injection (NDC 25021-241-10) due to failed impurities and degradation specifications.
FDA•LOWPrimidone Tablets 50 mgGolden State Medical Supply is recalling Primidone Tablets 50 mg due to cross-contamination with trace amounts of Acemetacin API.
2 products
FDA•LOWPrimidone 250mg TabletsLannett Company is recalling Primidone 250mg Tablets (NDC 0527-1231-01) due to potential cross-contamination with Acemetacin API.
FDA•CRITICALMG217 Multi-Symptom Treatment CreamWisconsin Pharmacal is recalling MG217 Multi-Symptom Treatment Cream due to Staphylococcus aureus contamination.
FDA•CRITICALArrow Edge Hemodialysis Catheterization KitArrow recalls hemodialysis kits over sheath introducer splitting failure risk.
6 products
FDA•CRITICALMedline Namic Angiographic Control Syringe KitsWindstone Medical is recalling Medline Namic Angiographic Control Syringe kits due to a risk of adapter disconnection and potential injury.
FDA•CRITICALNamic Angiographic ManifoldMedline recalls Namic Angiographic Manifolds (SKU 64038200) over particulate in fluid path.
14 products
NHTSA•CRITICALFontaine Fusion Flatbed Trailer Main BeamsFontaine is recalling 2025–2026 Fusion flatbed trailers; main beams may crack due to hydrogen contamination during galvanization.
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 trail mixes over possible Salmonella contamination.
6 products
FDA•LOWBuspirone Hydrochloride TabletsUnichem is recalling 5 mg buspirone hydrochloride tablets due to subpotency, which may reduce the medication's effectiveness.
FDA•CRITICALBeacon Tip Centimeter Sizing CatheterCook recalls Beacon Tip Centimeter Sizing Catheters due to risk of marker band cracking and device fragmentation.
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•LOWPALAMIX duo / PALAMIX unoHeraeus recalls PALAMIX duo and uno mixing units due to risk of mixing rod loosening in units over 17 months old.
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•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 is recalling Bette's Bake Sale bonbons due to an undeclared walnut allergen caused by mislabeled tasting guides.
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.
FSIS•CRITICALAjinomoto Chicken and Pork ProductsAjinomoto is recalling 36.9M lbs of chicken and pork fried rice, ramen, and shu mai products nationwide over possible foreign matter contamination.
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 over air bubble risk.
6 products
FDA•LOWIsland Kinetics: multiple drugsIsland Kinetics recalls three hydrocortisone 1% gels due to subpotency.
3 products
FDA•CRITICALBlaine Labs: multiple drugsBlaine Labs recalls Revitaderm Wound Care Gel and other products over microbial contamination.
9 products
FDA•CRITICALMagnesium Sulfate in Water for Injection IV BagAmneal is recalling Magnesium Sulfate IV bags (NDC 70121-1720-3) due to product mix-up with Tranexamic Acid.
FDA•CRITICALMedline Convenience Kits with Namic RA SyringesMedline recalls convenience kits with Namic RA syringes due to risk of loose connection or disconnection during use.
25 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.
- Device RecallFDA•CRITICALPhilips Respironics Trilogy Evo Ventilator
Philips Respironics recalls Trilogy Evo ventilators over delayed obstruction alarm.
4 products 
FDA•CRITICALCentrosFLO Hemodialysis CathetersMerit Medical recalls 80+ CentrosFLO hemodialysis catheter variants over sheath introducer splitting defect.
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•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 recalls Flexible Cryoprobes (REF 20402-401) due to rupture/burst risk.
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•CRITICALMiss Vickie's Spicy Dill Pickle ChipsMiss Vickie's is recalling 8 oz bags of Spicy Dill Pickle chips due to an undeclared milk allergen.
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.
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 Capsules (150 mg, 200 mg) over failed stability tests for appearance.
2 products
FDA•CRITICALImpella RP Flex with SmartAssistAbiomed recalls Impella RP Flex with SmartAssist due to sensor drift risk.
3 products
FDA•CRITICALNavitas Organics Organic Chia SeedsNavitas Organics is recalling 8 oz packages of Organic Chia Seeds due to potential Salmonella contamination.
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.