FDA•
TNVitamins and Doctor’s Pride Moringa Capsules
TNVitamins and Doctor’s Pride are recalling Moringa capsules over potential Salmonella contamination.
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FDA•MODERATENiacin Extended-Release Tablets 1,000 mgGolden State Medical Supply is recalling Niacin Extended-Release Tablets 1,000 mg due to failed dissolution specifications.
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 is recalling Halyard Pain Packs because the pouches did not undergo validated sterilization, posing an infection risk.
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 is recalling various CSK Electrodes because the reusable devices may not meet expected performance levels.
2 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.
FDA•LOWPrimidone 50 mg TabletsAmneal Pharmaceuticals is recalling Primidone 50 mg tablets due to potential cross-contamination with Acemetacin API.
FDA•Minocycline Hydrochloride 115 mg TabletsAscend Laboratories is recalling Minocycline Hydrochloride 115 mg tablets due to failed dissolution specifications.
FDA•Neuro Nourish Dietary SupplementSensory Supplement is recalling Neuro Nourish dietary supplement due to premature lipid oxidation causing an off odor and bitter taste.
FDA•MODERATEZep Alcohol Sanitizer SprayZep Inc. is recalling 55-gallon containers of Alcohol Sanitizer Spray due to potential microbial contamination.
FDA•MODERATEAdvance Aluminum Chloride Gel Hemostatic KitInter-Med is recalling Aluminum Chloride Gel kits due to an incorrect package insert that provides dangerous first aid instructions.
FDA•MODERATEDragonfly Thai Ginger PowderDragonfly Thai Ginger Powder is being recalled due to potential lead contamination.
FDA•MODERATEHintermann Series Talar ImplantDT MedTech is recalling the Hintermann Series Talar Implant due to a labeling error that may result in the wrong implant being used.
FDA•MODERATESiemens Dimension Tacrolimus Flex Reagent CartridgeSiemens is recalling Dimension Tacrolimus Flex reagent cartridges due to a potential positive bias in test results.
FDA•MODERATEPark St. Deli Macaroni & CheesePark St. Deli Macaroni & Cheese is recalled due to an undeclared soy lecithin allergen.
FDA•Clover Hill Dairy Soft Ricotta/Requeson CheeseClover Hill Dairy is recalling Soft Ricotta/Requeson Cheese due to potential Listeria monocytogenes contamination.
FDA•LOWPasteurized Donor Human MilkMothers' Milk Bank of Louisiana is recalling 3 oz bottles of donor human milk due to potential physical contamination.
FDA•Beekeeper's Naturals Saline Nasal SprayBeekeeper's Naturals is recalling 1 FL OZ Saline Nasal Spray bottles due to potential microbial contamination.
FDA•LOWEstrella Passion Fruit DrinkRefresqueria Estrella is recalling Passion Fruit Drink in 14 oz, 64 oz, and 120 oz bottles due to undeclared FD&C Red 40.
FDA•MODERATEFarm Rich Pizza Cheese CrunchersRich Products Corp is recalling Farm Rich Pizza Cheese Crunchers due to potential metal contamination.
FDA•MODERATEMedartis APTUS Cannulated Compression ScrewsMedartis is recalling APTUS cannulated compression screws due to a manufacturing defect where the cannulation is not centered.
FDA•MODERATEEXENT AnalyserThe Binding Site is recalling the EXENT Analyser due to a software error that may cause inaccurate M-protein detection or measurements.
FDA•MODERATEBrazo Gitano Caramel Sweet RollGalaxy RG Corp is recalling Brazo Gitano Caramel Sweet Roll due to undeclared Yellow #5, Yellow #6, and Red #40 food dyes.
23 products
NHTSA•MODERATEFord Expedition Center ConsoleFord is recalling 2018–2024 Expedition vehicles because peeling chrome on the center console can create sharp edges, increasing injury risk.
NHTSA•MODERATEFord Mustang, Lincoln Nautilus, and Navigator Instrument ClusterFord is recalling 2019 Mustang, Nautilus, and Navigator vehicles because the instrument cluster may go blank, failing to show safety data.
NHTSA•MODERATEFord Explorer Powertrain Control ModuleFord is recalling 2024 Explorer vehicles with 2.3L engines over a PCM reset issue that can cause a vehicle rollaway risk.
NHTSA•MODERATEFord Focus Canister Purge ValveFord is recalling 2012–2018 Focus vehicles due to a faulty canister purge valve that may cause the engine to stall while driving.
FDA•Steve's Real Food Chicken Recipe Freeze DriedSteve's Real Food is recalling its Chicken Recipe Freeze Dried pet food due to inadequate thiamine levels for cats.
FDA•Budesonide Inhalation SuspensionSun Pharmaceutical is recalling Budesonide Inhalation Suspension due to the presence of foreign particles in the solution.
FDA•MODERATEDuloxetine Delayed-Release Capsules 30mgBreckenridge Pharmaceutical is recalling 30mg Duloxetine capsules due to levels of N-nitroso-duloxetine impurity exceeding FDA limits.
2 products
FDA•MODERATENeoSpan SuperElastic Compression StapleIn2bones USA is recalling 10+ variants of NeoSpan compression staples due to missing MR Conditional safety labeling.
FDA•LOWWeiKFiELD Custard Powder Kesar PistaWeikfield is recalling 300g jars of Custard Powder Kesar Pista due to a labeling error regarding the ingredient Pistachio.
- Drug RecallFDA•BD ChloraPrep and FREPP Applicators
BD is recalling ChloraPrep and FREPP applicators distributed nationwide due to potential fungal contamination.
FDA•Requeson CheeseNelson & Isa Lacteos is recalling 1lb. packages of Requeson cheese due to potential Listeria monocytogenes contamination.
FDA•LOWEpinephrine Injection 1mg/mLFresenius Kabi is recalling Epinephrine Injection 1mg/mL vials due to out-of-specification stability test results.
FDA•MODERATEPhilips DigitalDiagnost C90 Wall StandPhilips is recalling DigitalDiagnost C90 systems because the Wall Stand VS2 lacks a required seismic stability kit.
FDA•MODERATEMicromed SD LTM 64 PLUS EEG AmplifierMicromed is recalling SD LTM 64 PLUS EEG amplifiers due to a potential one-second temporal delay that may cause misinterpretation of results.
FDA•MODERATECGuard Prime Carotid Stent SystemInspireMD is recalling the CGuard Prime Carotid Stent System (Model CND0830) due to potential deployment complications.
6 products
FDA•CRITICALDoxorubicin Hydrochloride Liposome InjectionNorthstar Rx is recalling Doxorubicin Hydrochloride Liposome injection 50 mg/25 mL vials due to potential glass particulate contamination.
FDA•MODERATECORFLO Safety PEG KitAvanos Medical is recalling the CORFLO Safety PEG Kit (model 30-4320) due to a quality issue with an included lidocaine injection component.
20 products
FDA•MODERATEMahurkar Elite PASS TraysMozarc Medical is recalling Mahurkar Elite PASS Trays because the Tegaderm CHG dressing is missing from the packaging.
FDA•MODERATEGE Allia IGS 3 Pulse Angiographic X-ray SystemGE is recalling the Allia IGS 3 Pulse X-ray system due to an electrical shock hazard for service personnel during maintenance.
5 products
FDA•MODERATEBicarby DialysateFresenius Medical Care is recalling Bicarby Dialysate due to a luer-lock leak issue that poses a slip and fall hazard.
FDA•MODERATEPlum Solo Precision IV PumpICU Medical is recalling the Plum Solo Precision IV Pump due to a software error that may cause inaccurate medication delivery.
3 products
FDA•MODERATED.O.R.C. TDC Veloce 23G Two Dimensional CutterD.O.R.C. is recalling 23G Two Dimensional Cutters because the outer knife may become loose during use, posing a risk of patient injury.
3 products
FDA•MODERATEEXCOR Pediatric VAD Blood Pump PU ValvesBerlin Heart is recalling EXCOR Pediatric VAD Blood Pump PU Valves due to an expiration date mismatch that could delay surgical procedures.