FDA•MODERATE
Philips Allura Xper FD20 Biplane X-Ray System
Philips is recalling Allura Xper FD20 Biplane X-ray systems due to potential foot switch failure causing intermittent or no imaging.
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FDA•MODERATEOXOID Microbact 12L Listeria Identification KitOxoid is recalling Microbact 12L Listeria Kit (MB1128A, Lot 4494873) due to risk of incorrect organism identification from ambiguous color reactions.
NHTSA•MODERATEFord EGR ValveFord is recalling 2025 Ranger, Nautilus, Mustang, Maverick, Explorer, Escape, Corsair, Bronco Sport, and Bronco vehicles over EGR valve failure causing loss of drive power.
NHTSA•MODERATEFord Bronco and Edge Accessory Protocol Interface ModuleFord is recalling 2021–2026 Bronco and 2021–2024 Edge vehicles; APIM overheating may disable rearview camera display.
NHTSA•MODERATEFord Escape, Corsair, Aviator, Explorer Rearview CameraFord is recalling Escape, Corsair, Aviator, and Explorer vehicles (2020–2024) for inverted rearview camera images that reduce rear visibility.
NHTSA•MODERATEFord Explorer Passenger-Side HeadlightFord is recalling 2025–2026 Explorer vehicles; passenger-side headlight may turn incorrectly in curves, increasing crash risk.
NHTSA•MODERATEFord Explorer, Escape, Aviator, Corsair Windshield Wiper MotorFord is recalling 2020–2022 Explorer, Escape, Aviator, and Corsair vehicles for windshield wiper motor failure that may reduce visibility.
NHTSA•MODERATEFord F-250 SD and F-350 SD DriveshaftFord is recalling 2026–2025 F-250 SD and F-350 SD vehicles over driveshaft separation risk.
NHTSA•MODERATEFord E-350 and E-450 Backup Alarm ConnectorFord is recalling 2026–2027 E-350 and E-450 vehicles; backup alarm connector may detach, silencing the reversing alert.
NHTSA•MODERATELincoln Navigator Driver's SeatFord is recalling 2026 Lincoln Navigator vehicles due to driver's seat reversing unexpectedly at low speeds.
FDA•MODERATEFarmhouse Fresh Midnight Clearing Night LotionFarmhouse Fresh is recalling Midnight Clearing Night Lotion acne treatment due to benzene contamination.
4 products
FDA•MODERATEInstinct Plus Endoscopic Clipping DeviceWilson-Cook Medical is recalling the Instinct Plus Endoscopic Clipping Device due to a potential for the device to malfunction.
FDA•MODERATESoft-Vu Angiographic CatheterAngiodynamics is recalling Soft-Vu angiographic catheters due to a manufacturing defect that may block guidewire passage.
20 products
FDA•MODERATEChina Noodle Co. Steam NoodlesChina Noodle Co. is recalling Steam Noodles due to undeclared wheat, which poses a risk to consumers with wheat allergies.
4 products
FDA•MODERATEChildren's Ibuprofen Oral Suspension 100 mg/5mLTaro Pharmaceuticals is recalling Children's Ibuprofen Oral Suspension 100 mg/5mL (120 mL) due to gel-like masses and black particles.
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•MODERATEeTRAX Needle System Starter KitCivco is recalling the eTRAX Needle System Starter Kit 18G due to a programming error that may cause incorrect needle tip positioning.
8 products
FDA•CRITICALPhilips Respironics Trilogy Evo VentilatorPhilips Respironics is recalling Trilogy Evo ventilators (software v1.05.15.00) due to potential tidal volume delivery inaccuracies.
4 products
FDA•CRITICALPhilips Respironics Trilogy Evo VentilatorPhilips Respironics is recalling Trilogy Evo O2 ventilators because the obstruction alarm may fail to trigger within the required timeframe.
4 products
FSIS•MODERATEPunahele Jerky Company Beef CrispsPunahele Jerky Company beef crisps (6-oz and 4-oz packages) contain undeclared soy lecithin allergen; best-by date Feb 17, 2027 or prior.
FDA•MODERATESavannah Bee Company Honey BBQ Sauce MustardSavannah Bee Company is recalling Honey BBQ Sauce Mustard due to undeclared soy and wheat allergens from mislabeling.
FDA•MODERATEDivided Sunset Multi Collagen PeptidesDivided Sunset Multi Collagen Peptides are recalled for undeclared egg and fish allergens.
FDA•MODERATESIGNA Premier MR Scanner Magnet FittingsGE Healthcare is recalling SIGNA Premier MR scanners due to ferrous magnet fittings that could cause personnel injury during service.
FDA•CRITICALNAMIC Angiographic Syringe Convenience KitsMedline is recalling NAMIC angiographic syringe kits due to a risk of the rotating adaptor unwinding and disconnecting during use.
24 products
FDA•MODERATEOlympus SOLTIVE Premium Laser SystemOlympus is recalling the SOLTIVE Premium Laser System due to a power supply defect that may cause the device to fail or emit smoke.
2 products
FDA•MODERATECardinal Health Monoject Tuberculin Syringe 1 mLCardinal Health is recalling Monoject Tuberculin Syringes (Catalog 1180100777) that contain U-100 insulin syringes instead, risking dosing errors.
FDA•MODERATESpacelabs Multi-parameter Command Module Model 91496Spacelabs is recalling Model 91496 Multi-parameter Command Module due to circuit board issue causing inaccurate cardiac output readings.
FDA•MODERATEMedline Convenience Kits with 10mL SyringesMedline is recalling 10+ convenience kit models containing 10mL syringes due to unapproved design changes.
21 products
FDA•CRITICALHouse of Flavors Chicago Vanilla Ice CreamHouse of Flavors is recalling 3-gallon tubs of Chicago Vanilla Ice Cream due to an undeclared egg allergen.
FDA•MODERATEPepsin 1:3000 PowderAmerican Laboratories is recalling Pepsin 1:3000 Powder due to potential Salmonella contamination.
3 products
FDA•CRITICALButter-Rich PowderBluegrass Ingredients is recalling 50 lb. bags of Butter-Rich Powder due to potential Salmonella contamination.
2 products
FDA•MODERATELevothyroxine Sodium Tablets USP 150 mcgMacleods Pharma recalls Levothyroxine Sodium 150 mcg tablets (NDC 33342-401-44) nationwide due to subpotency.
FDA•MODERATENomida Semaglutide InjectionNew Life Pharma is recalling Nomida Semaglutide Injection due to a lack of assurance of sterility.
4 products
NHTSA•MODERATEAcura ZDX and Prologue Instrument Panel and Rearview Camera DisplayHonda is recalling 2024 Acura ZDX and Prologue vehicles for instrument panel display failure and rearview camera blank-screen defects that increase crash risk.
NHTSA•MODERATEBMW S 1000 RR Turn SignalBMW is recalling the 2026 S 1000 RR motorcycle due to turn signal malfunction that increases crash risk.
NHTSA•MODERATEBuick Regal Rear Toe LinkGM is recalling 2012–2013 Buick Regal Turbo and GS models over rear toe link fracture risk that may cause loss of vehicle control.
NHTSA•MODERATEGeneral Motors Multiple Models Electronic Owner's ManualGM recalling 2025–2027 Chevrolet, Cadillac, GMC, and Buick models over missing electronic owner's manual.
NHTSA•MODERATEIC Bus CESB School Bus Brake LinesInternational is recalling 2023–2027 IC Bus CESB school buses; brake lines may leak due to incorrect hardware installation.
FDA•MODERATELowes Foods Sour Cream and Onion Potato ChipsLowes Foods sour cream and onion potato chips recalled for inaccurate nutrition labels and undeclared MSG.
FDA•CRITICALDreamland Zaatar Chickpea SaladDreamland Zaatar Chickpea Salad is recalled for undeclared sesame, soy, and wheat allergens found in grab-and-go containers.
2 products
FDA•LOWC2O Coconut Water with PulpC2O Coconut Water with Pulp is recalled due to an incorrect ingredient label on the outer box that omits added sugar content.
FDA•MODERATESynthes 2.4 Volt Locking Screw TapSynthes is recalling 2.4 Volt Locking Screw Taps (Part 03.424.124-US) due to a packaging error resulting in incorrect thread dimensions.
2 products
FDA•MODERATEOlympus PKS Cutting ForcepsOlympus is recalling PKS Cutting Forceps (model 3005PK) because a welding defect may cause the device's jaw to break during use.
7 products
NHTSA•MODERATEEvenflo LiteMax Factory Select Child SeatEvenflo LiteMax Factory Select (model CS100111198) recalled for incorrect weight/height limits in Spanish manual.
NHTSA•MODERATEToyota Corolla Headlight AssemblyToyota is recalling 2026 Corolla vehicles with missing headlight aim markings that may reduce visibility or create glare.
FDA•MODERATEMedline Namic GuidewiresMedline is recalling 50+ Namic guidewires, syringes, and tubing products due to rescinded 510(k) regulatory clearances.
28 products
FDA•MODERATEGreenway Farms Jalapeno Dill Pickle ChipsGreenway Farms is recalling 16 fl oz Jalapeno Dill Pickle Chips due to the lack of a required process authority.
2 products
FDA•MODERATEKing Harvest HummusKing Harvest is recalling Jalapeno and Roasted Red Pepper Hummus in 10 oz and 17 oz tubs due to potential aluminum piece contamination.
6 products
FDA•MODERATEImu-Tek Colostrum-5 CapsulesImu-Tek is recalling Colostrum-5 120-count capsules due to potential under-processing.
2 products
FDA•MODERATEAmnesteem Isotretinoin Capsules 40 mgMylan is recalling Amnesteem Isotretinoin 40 mg capsules (NDC 0378-6614-93) due to failed dissolution specifications.