FDA•CRITICAL
Taro Cakes
E & S Grocery & Bakery is recalling Taro Cakes due to an undeclared egg allergen.
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FDA•MODERATEPhilips MultiDiagnost Eleva Hand SwitchPhilips recalls MultiDiagnost Eleva systems over hand switch that may not release, risking unintended radiation.
3 products
FDA•MODERATENutrisystem Chocolate CheesecakeNutrisystem is recalling Chocolate Cheesecake 2 oz packages due to an undeclared soy allergen.
FDA•CRITICALAl Yaman Halawa Extra PistachioAl Yaman Halawa Extra Pistachio 907g jars recalled over possible Salmonella contamination.
FDA•MODERATEGreat Value Hawaiian Roll 4pkGreat Value Hawaiian Roll 4pk recalled over oily substance on food-contact packaging; product never reached store shelves.
FDA•MODERATERitmed Neurological SpongesAMD Medicom recalls Ritmed Neurological Sponges due to elevated endotoxin risk; full REF list on FDA page.
2 products
FDA•MODERATEdirectCHECK ACT-LR Whole Blood Quality ControlAccriva Diagnostics is recalling directCHECK ACT-LR whole blood quality control, level 2, due to incorrect performance range labeling.
FDA•MODERATEMID DOLCIARIA SRL: 2 Via Casalini BelpassosMID DOLCIARIA recalls Cannoli Siciliani and Crunchy Cannoli Gluten Free over unapproved colors E140/E141.
2 products
FDA•MODERATETrigen Proximal Straight Humeral NailSmith & Nephew is recalling the Trigen Proximal Straight Humeral Nail due to a manufacturing error that may cause surgical delays or revision.
NHTSA•MODERATEStoryteller GXV Hilt Alternator PulleyStoryteller is recalling 2024-2026 GXV Hilt vehicles due to an alternator pulley failure that may cause a loss of power brakes and steering.
FDA•CRITICALFirst Street Dark Chocolate RaisinsFirst Street Dark Chocolate Raisins are recalled due to undeclared peanuts, which pose a risk to consumers with peanut allergies.
FDA•MODERATEAripiprazole 30 mg TabletsAjanta Pharma is recalling Aripiprazole 30 mg tablets due to a mix-up with Voriconazole 50 mg tablets.
FDA•MODERATEMedtronic O-arm O2 Imaging SystemMedtronic is recalling the O-arm O2 Imaging System due to a firmware anomaly that may cause image artifacts during clinical use.
FDA•MODERATEHarmonyAIR A-Series Surgical Lighting SystemHarmonyAIR A-Series surgical lights recalled: intensity buttons may detach.
2 products
FDA•MODERATEHarmonyAIR A-Series Surgical Lighting SystemSteris is recalling HarmonyAIR A-Series Surgical Lighting Systems due to a risk of paint delamination on the light heads.
NHTSA•MODERATEForest River XLR Toy Hauler Recreational TrailersForest River is recalling 2023-2024 XLR Toy Hauler trailers due to an incorrect GVWR that may lead to vehicle overloading and crash risk.
NHTSA•MODERATEWabash 2027 Van Trailer Rear Impact GuardWabash is recalling 2027 van trailers due to improperly tightened rear impact guard bolts that may fail to meet federal safety standards.
FDA•CRITICALNara Organics Whole Milk Organic Infant FormulaNara Organics is recalling Whole Milk Organic Infant Formula over potential Clostridium botulinum contamination.
- Equipment RecallNHTSA•MODERATEWaymo 5th Generation Automated Driving Systems
Waymo is recalling 5th Generation ADS software that may allow vehicles to enter and drive through closed freeway construction zones.
FDA•MODERATEPepperoni Rolls 5 ozPepperoni Rolls recalled for undeclared milk allergen and improper refrigeration; 5 oz packages.
FDA•MODERATEDabur India: Multiple Made In India ProductsDabur India recalls 14 OTC topical products over CGMP deviations.
14 products
FDA•MODERATEChlorthalidone 25 mg TabletsChlorthalidone 25 mg tablets are being recalled due to failed dissolution specifications.
FDA•LOWFocalin XR 5 mg CapsulesSandoz is recalling Focalin XR 5 mg capsules due to missing or incorrect lot numbers and expiration dates on the product labels.
FDA•MODERATEAlyacen 7/7/7 TabletsGlenmark is recalling Alyacen 7/7/7 tablets due to out-of-specification results for total impurities.
FDA•MODERATEVasopressin 2 Units/2 mL SyringesIntegraDose is recalling Vasopressin 2 Units/2 mL syringes due to subpotency, which may cause the drug to be ineffective.
FDA•MODERATEPAI: Multiple Kerr Insta-char In An ProductsVistaPharm recalls Kerr Insta-Char activated charcoal (25g/50g) for failing OTC monograph requirements.
4 products
FDA•MODERATEMedline EBSI KitMedline recalls EBSI Kit (EBSI1534) due to cracked butyrate tubing and recalled MASTISOL adhesive.
42 products
FDA•CRITICALImpella Heart Pump Software RecallAbbott's Impella heart pumps may fail to restart after certain operational faults, posing a serious health risk to patients.
2 products
FDA•CRITICALParacentesis KitArrow International recalls paracentesis kits due to supplier quality issues with included injectables, risking serious injury.
51 products
NHTSA•MODERATEWinnebago Revel and Revel Sport Recreational VehiclesWinnebago is recalling 2026-2027 Revel and Revel Sport RVs due to incorrect tire information labels that may lead to improper tire installation.
NHTSA•MODERATEThomas Built SAF-T-LINER HDX2 School Bus Body JointsDaimler is recalling 2027 Thomas Built SAF-T-LINER HDX2 school buses due to insufficient body joint strength that may increase injury risk.
NHTSA•MODERATEKawasaki W230 Motorcycle Turn Signal BulbsKawasaki is recalling 2025-2026 W230 motorcycles due to defective turn signal bulbs that may fail and increase the risk of a crash.
NHTSA•MODERATEAltec AT Series Aerial DeviceAltec is recalling 2014-2026 AT Series Aerial Devices because a missing transmission park interlock may cause unexpected vehicle movement.
NHTSA•MODERATEWaltco MDV Series Liftgate Deck PinsMarion Body Works is recalling Waltco MDV series liftgates on Morgan dry vans because broken deck pins may cause the platform to fall.
NHTSA•MODERATELand Rover Defender, Discovery, and Range Rover Air BagLand Rover is recalling various 2020-2026 Defender, Discovery, and Range Rover vehicles due to an air bag clockspring corrosion risk.
FDA•CRITICALAzuma Foods Tako Wasabi Seasoned OctopusAzuma Foods is recalling Tako Wasabi Seasoned Octopus due to undeclared fish.
FDA•MODERATENiacin Extended-Release Tablets 1,000 mgGolden State Medical Supply is recalling Niacin Extended-Release Tablets, 1,000 mg, due to failure to meet dissolution specifications.
2 products
FDA•MODERATEFresh Roast Systems ColorTrack InstrumentFresh Roast Systems is recalling the ColorTrack instrument (Model BENCH R-100) due to a potential laser safety hazard.
FDA•MODERATEHalyard Pain PackAVID Medical recalls Halyard Pain Pack kits (AMPK48-01) over possible lack of sterilization.
4 products
FDA•MODERATEMOSAIQ Oncology Information SystemElekta is recalling the MOSAIQ Oncology Information System due to a software error that may prevent the loading of baseline shift plans.
FDA•MODERATEBoston Scientific Orca Air/Water and Suction ValvesBoston Scientific is recalling Orca single-use air/water and suction valves due to reports of the suction button sticking during use.
- Device RecallFDA•MODERATEMerlin Patient Care System Programmer Software
Abbott Medical is recalling Merlin PCS software for the Model 3330 programmer due to a potential failure to terminate pacing tests.
FDA•MODERATEBoston Scientific Clik X AnchorBoston Scientific is recalling the Clik X Anchor due to a potential lack of sterility assurance.
FDA•MODERATEBoston Scientific CSK ElectrodesBoston Scientific recalls CSK reusable electrodes over performance concerns.
4 products
FDA•MODERATEBicarby DialysateFresenius Medical Care is recalling Bicarby Dialysate due to a GTIN labeling error that may result in the use of an incorrect potassium solution.
NHTSA•MODERATEGreat Dane Champion Dry Van TrailersGreat Dane is recalling 2026 Champion dry van trailers because broken deck pins may cause the liftgate platform to fall.
NHTSA•MODERATEInternational HV Service BrakeInternational is recalling 2026-2027 HV vehicles due to a delayed service brake release that may increase the risk of a crash.
NHTSA•MODERATEAltec AC Series Crane Personnel JibAltec is recalling 2024-2026 AC Series Crane personnel jibs (IJ26) due to missing welds that may cause the platform to fall.
FDA•LOWPrimidone 50 mg TabletsAmneal Pharmaceuticals is recalling Primidone 50 mg tablets due to potential cross-contamination with Acemetacin API.
FDA•MODERATEMinocycline Hydrochloride 115 mg TabletsAscend Laboratories is recalling Minocycline Hydrochloride 115 mg tablets due to failed dissolution specifications.