FDA•LOW
Buspirone Hydrochloride Tablets
Unichem is recalling 5 mg buspirone hydrochloride tablets due to subpotency, which may reduce the medication's effectiveness.
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FDA•CRITICALHalyard Cardiac Cath Pack KitAVID Medical recalls Halyard Cardiac Cath Pack kits over risk of syringe adaptor disconnection.
10 products
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•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
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 O2 Ventilator
Philips Respironics recalls Trilogy Evo O2 ventilators (SW 1.05.15.00) over delayed obstruction alarm.
4 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•CRITICALMiss Vickies Spicy Dill Pickle ChipsFrito-Lay recalls Miss Vickies Spicy Dill Pickle chips 8 oz bags for 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.
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.
NHTSA•CRITICALSubaru Crosstrek Hybrid and Forester Hybrid Fuel CapSubaru is recalling 2026 Crosstrek hybrid and 2025 Forester hybrid vehicles over fuel cap seal defect that may cause fuel leakage and fire risk.
FSIS•CRITICALBremer Italian Style MeatballsRosina recalls frozen Bremer Italian Style Meatballs over possible metal contamination.
FDA•LOWSodexo Stars Saccharin PacketsDomino Foods recalls Sodexo Stars Saccharin Packets due to undeclared aspartame.
FDA•CRITICALUdenyca Pegfilgrastim-cbqv InjectionAccord BioPharma is recalling Udenyca injection due to improper storage temperature conditions.
FDA•CRITICALOlympus High Flow Insufflation UnitOlympus is recalling the UHI-3 High Flow Insufflation Unit due to a software issue that may cause dangerous overpressure events.
3 products
NHTSA•CRITICALFord Transit Brake PedalFord is recalling 2025 Transit vehicles; brake pedal may disconnect, causing loss of brake function.
FDA•CRITICALRosabella Moringa Dietary Supplement CapsulesAmbrosia Brands is recalling Rosabella Moringa dietary supplement capsules due to potential Salmonella contamination.
FDA•LOWDoxazosin Tablets, USP 4 mgUnichem is recalling Doxazosin Tablets 4 mg (NDC 29300-353-10) due to incorrect tablet imprinting that may cause medication errors.
FDA•LOWStraumann WB Impression Post Closed TrayStraumann is recalling WB Impression Post Closed Tray kits (L 13mm) due to incorrect magenta impression caps instead of brown.
FDA•CRITICALTRUE METRIX Blood Glucose Meter InstructionsTrividia recalls TRUE METRIX meter instructions over inadequate E-5 error guidance.
7 products