FDA•MODERATE
Remel GC Agar Base
Remel is recalling GC Agar Base plates due to a risk of reduced or no recovery of Neisseria gonorrhoeae strains.
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FDA•CRITICALHamilton Medical Ventilator Coaxial Breathing CircuitHamilton Medical is recalling ventilator coaxial breathing circuits due to a risk of valve membrane adhesion and inadequate ventilation.
NHTSA•MODERATEEntegra Accolade and Jayco Seneca MotorhomesJayco is recalling 2027 Entegra Accolade and Jayco Seneca motorhomes because missing dinette brackets may cause the seating to detach.
NHTSA•MODERATETeko Triumph, Turbo, and Trophy VehiclesTeko is recalling 2026 Triumph, Turbo, and Trophy vehicles because a missing alert system prevents them from making required pedestrian sounds.
NHTSA•MODERATEJATCO Automatic Transmission Control Valve AssemblyNissan is recalling JATCO automatic transmission control valve assemblies that may fail to correctly display the selected gear.
NHTSA•MODERATELincoln Nautilus Hybrid and Explorer HybridFord is recalling certain 2024-2027 Lincoln Nautilus Hybrid and 2025-2027 Explorer Hybrid vehicles due to a missing pedestrian warning sound.
NHTSA•MODERATEFord Mustang and Mustang GTD Windshield WipersFord is recalling 2024–2026 Mustang and 2025–2026 Mustang GTD vehicles because cold weather can cause windshield wiper and washer malfunctions.
NHTSA•MODERATEFord Mustang Mach-E Rear Differential Pinion ShaftFord is recalling 2021-2023 Mustang Mach-E vehicles due to a risk of rear differential pinion shaft fracture and potential loss of drive power.
NHTSA•MODERATENissan Rogue Instrument PanelNissan is recalling 2026 Rogue vehicles because the instrument panel may fail to display the gear selection, increasing the risk of a crash.
NHTSA•MODERATEJeep Grand Wagoneer Brake System Control ModuleChrysler is recalling 2026 Jeep Grand Wagoneer and Grand Wagoneer L vehicles due to a software error that may cause a loss of brake assist.
2 products
NHTSA•MODERATEJeep Grand Cherokee and Wagoneer Transmission IndicatorChrysler is recalling certain 2022-2024 Jeep Grand Cherokee and Wagoneer vehicles due to a software error affecting the gear selection indicator.
FDA•LOWFexofenadine Hydrochloride Tablets 180 mgOhm Laboratories is recalling 180 mg Fexofenadine Hydrochloride tablets due to failed impurities and degradation specifications.
FDA•CRITICALBosco's Blend Chicken Doggone RawDoggone Raw is recalling 2 lb and 10 lb tubs of Bosco's Blend Chicken Doggone Raw due to potential Salmonella contamination.
FDA•MODERATEImuldosa (ustekinumab-srlf) InjectionAccord BioPharma is recalling Imuldosa (ustekinumab-srlf) 130 mg/26 mL injection vials due to a lack of assurance of sterility.
FDA•MODERATELe Chef Bakery: 2 productsLe Chef Bakery recalls Mini Tiramisu and Mini Italian Pastry Assortment due to undeclared Yellow #5.
2 products
FDA•MODERATEOribe Serene Scalp Densifying ShampooOribe Serene Scalp Densifying Shampoo recalled due to microbial contamination.
FDA•MODERATEMedline Convenience Kits with LidocaineMedline recalls 3 convenience kits with Huons Lidocaine ampules due to quality issues.
19 products
FDA•MODERATEATTUNE Knee System Revision Hinge Housing ComponentsDePuy Synthes (Johnson & Johnson) is recalling the ATTUNE Knee System Revision Hinge Housing Components due to a risk of fracture.
4 products
FDA•MODERATEMedacta Shoulder System Short Monobloc Stem BroachesMedacta is recalling Short Monobloc Stem Broaches for the Shoulder System due to a risk of humerus fracture during surgery.
NHTSA•MODERATETiffin Recreational Vehicle MaxxAir Rooftop FansTiffin is recalling various 2026-2027 recreational vehicles equipped with MaxxAir N-Series rooftop fans due to an overheating fire risk.
2 products
NHTSA•MODERATEJayco Alante and Entegra Vision Recreational VehiclesJayco is recalling 2024 Alante and Entegra Vision RVs due to incorrect weight labels that may lead to vehicle overloading.
FDA•CRITICALLa Colonia Foods: 4 productsLa Colonia Foods is recalling Ricotta and other fresh cheeses over possible Listeria contamination.
4 products
FDA•CRITICALTNVitamins Organic Moringa Capsules and PowderTNVitamins Organic Moringa Capsules and Powder recalled due to possible Salmonella contamination.
FDA•CRITICALDiclofenac Sodium 0.1% Eye OintmentMFV Compounding Pharmacy is recalling Diclofenac Sodium 0.1% Eye Ointment due to potential Bacillus cereus contamination.
FDA•MODERATEBlue Ribbon Classics French Vanilla Ice Cream (1 gal)Wells Enterprises recalls Blue Ribbon Classics French Vanilla (1 gal) due to elevated coliforms.
3 products
FDA•MODERATEMedline Convenience Kits with Swan-Ganz CathetersMedline recalls convenience kits with BD Swan-Ganz catheters due to hub failure risk.
9 products
FDA•MODERATEMentor Luer Lok 10cc SyringesMentor is recalling a lot of 10cc Luer Lok syringes that were distributed after their expiration date.
NHTSA•MODERATEDiamond Coach VIP Motorcoach Wheelchair RetractorDiamond Coach is recalling 2025-2026 VIP motorcoaches with QRT-360 wheelchair retractors that may fail to lock, increasing injury risk.
NHTSA•MODERATE2025 Nissan Sentra DriveshaftNissan is recalling 2025 Sentra vehicles due to a potential driveshaft installation issue that may cause power loss or vehicle rollaway.
NHTSA•MODERATEAltec Digger Derrick Pole RackAltec is recalling 2023-2025 Digger Derrick vehicles due to an incorrect pole rack capacity rating that may increase the risk of a crash.
NHTSA•MODERATEThomas Built Saf-T-Liner HDX2 Entrance DoorDaimler Trucks is recalling 2026-2027 Thomas Built Saf-T-Liner HDX2 buses because the entrance door may fail to open or close.
- NHTSA•MODERATEThomas Built SAF-T-LINER School Bus Entrance Door
Daimler is recalling 2026-2027 Thomas Built SAF-T-LINER HDX2 and EFX2 school buses because the entrance door may fail to open or close.
FDA•CRITICALBreeder's Edge Foster Care GM Enriched Goat Milk FormulaRevival Animal Health is recalling Breeder's Edge Foster Care GM Enriched Goat Milk Formula due to elevated Vitamin D levels.
FDA•CRITICALHigh Valley Orchard Chocolate: 2 productsHigh Valley Orchard Chocolate Covered Raisins recalled over undeclared peanut allergen.
2 products
FDA•MODERATEBakr Brown Butter Chocolate Chunk Cookie DoughBakr Brown Butter Chocolate Chunk Cookie Dough recalled over undeclared soy allergen.
FDA•MODERATEPovi-One 10% Povidone-Iodine Oral AntisepticElevate Oral Care is recalling Povi-One 10% Povidone-Iodine Oral Antiseptic due to sub-potency.
FDA•MODERATEIntera 3000 Hepatic Artery Infusion PumpIntera 3000 Hepatic Artery Infusion Pump recalled over potential drug pathway leakage.
FDA•MODERATEMedline Convenience Kits with 10mL Polycarbonate SyringesMedline recalls convenience kits with 10mL polycarbonate syringes due to unapproved design changes.
23 products
FDA•CRITICALAbiomed Impella CP Introducer KitAbiomed recalls Impella CP introducer kit (14 Fr x 13 cm) over thrombus risk.
4 products
FDA•MODERATEPediatric Total Parenteral Nutrition BagCentral Admixture Pharmacy Services is recalling a pediatric TPN bag due to an incorrect formulation missing copper and famotidine.
FDA•MODERATEPerampanel CIII TabletsSun Pharmaceutical is recalling 6mg Perampanel CIII tablets due to a labeling mix-up where bottles may contain 10mg tablets.
FDA•MODERATELacosamide 100mg TabletsCamber Pharmaceuticals is recalling Lacosamide 100mg tablets due to a potential mix-up with Selexipag 1000 mcg tablets.
2 products
FDA•MODERATEEl David Gelee Bonbons with FruitsAlb-USA is recalling El David Gelee Bonbons with Fruits due to undeclared FD&C Yellow 5 and FD&C Red 40.
FDA•LOWHydroxyzine Hydrochloride Oral SolutionANI Pharmaceuticals is recalling Hydroxyzine Hydrochloride Oral Solution, 10 mg/5 mL, due to the presence of a foreign substance.
FDA•MODERATEPhilips Telemetry Monitor 5500Philips is recalling Telemetry Monitor 5500 units due to a potential reset error that prevents connection to the central monitoring system.
FDA•LOWLunch Box Kitchen Turkey & Cheddar SubLunch Box Kitchen Turkey & Cheddar Sub recall: mislabeled (may be roast beef & Swiss); BEST BY 06/14/26.
FDA•MODERATEPersona Revision Femoral Distal AugmentZimmer is recalling the Persona Revision Femoral Distal Augment (model 42-5572-066-10) due to a packaging error.
- Device RecallFDA•MODERATEThuvera Laser Console
IPG Medical is recalling the Thuvera Laser Console due to a software anomaly that may cause a false error code 5018 display.
FDA•CRITICALMedline CV Anesthesia Room Setup KitsMedline recalls CV Anesthesia Room Setup kits due to quality issues with included lidocaine and bupivacaine injections.
5 products
FDA•MODERATEGE Healthcare AW Server 3.2 ext.6.5GE Healthcare is recalling the AW Server 3.2 ext.6.5 image processing system due to a software error that may display the wrong patient's data.