FDA•CRITICAL
La Colonia Foods: 4 products
La Colonia Foods is recalling Ricotta and other fresh cheeses over possible Listeria contamination.
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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.
FDA•MODERATEPReye Vitamin See Antioxidant Eye DropsPReye is recalling Vitamin See Antioxidant Preservative Free Eye Drops due to a lack of assurance of sterility.
FDA•MODERATEOctopus Evolution Tissue StabilizerMedtronic recalls Octopus Evolution Tissue Stabilizer TS2000 due to incorrect tubing assembly.
3 products
FDA•MODERATESurgify Halo BurrSurgify Halo 3.0 mm burr recalled due to potential breakage during spinal surgery.
19 products
FDA•MODERATEStryker InZone Detachment SystemStryker is recalling the InZone Detachment System due to premature battery drain that may prevent coil detachment during medical procedures.
NHTSA•MODERATEAirstream Recreational Vehicle Maxxfan Ventilation FanAirstream is recalling certain 2026 Classic trailers and 2025-2027 Interstate RVs due to a fire risk from overheating Maxxfan circuit boards.
2 products
NHTSA•MODERATEHyundai Tucson Instrument Panel DisplayHyundai is recalling 2025-2026 Tucson vehicles due to a software error that may cause the instrument panel display to fail.
NHTSA•MODERATEFord Bronco Fender FlareFord is recalling 2022-2026 Bronco vehicles because improperly secured fender flares may detach, creating a road hazard.
NHTSA•MODERATEFord and Lincoln Transmission Park PawlFord is recalling various 2018-2021 Ford and Lincoln vehicles due to a transmission park pawl issue that may cause a vehicle rollaway.
NHTSA•MODERATEHarbinger Stripped Chassis Steering Gear BoltsHarbinger is recalling 2025 Stripped Chassis vehicles due to steering gear bolts that may loosen or break, increasing the risk of a crash.
2 products
NHTSA•MODERATEElgin Pelican High Voltage BatteryElgin is recalling 2024-2026 Pelican vehicles with Samsung SDI high voltage battery packs due to a fire risk from potential battery failure.
FDA•MODERATEDuloxetine Delayed-Release CapsulesDirect Rx is recalling 30 mg Duloxetine Delayed-Release capsules due to N-nitroso-duloxetine impurity levels exceeding FDA limits.
FDA•MODERATEAcumed Hexalobe ScrewsAcumed is recalling various hexalobe screws used in wrist fixation systems due to a risk of the screws breaking during use.
2 products
FDA•MODERATEAmgen Corlanor and Sensipar TabletsAmgen recalls Corlanor and Sensipar tablets over foreign substance contamination.
5 products
FDA•MODERATEZimmer Off-Axis Reamer GuideZimmer recalls Off-Axis Reamer Guide (Model 110040240) due to breakage risk from catching during reaming.
5 products
FDA•MODERATEJoy Gourmet Foods: 14 productsJoy Gourmet recalls Joy brand lassi drinks over inadequate pasteurization.
14 products
FDA•MODERATEPFM Medical Multi-Snare SetPFM Medical is recalling Multi-Snare Set catheter devices due to a failure to meet biocompatibility requirements for in-vitro cytotoxicity.
FDA•MODERATEVentec VOCSN+Pro Respiratory SystemVentec is recalling the VOCSN+Pro respiratory system because a damaged battery may prevent the backup alarm from sounding during power loss.
NHTSA•MODERATEGM Express and Savana Steering Gear AssemblyGM is recalling 2025-2026 Express and Savana vehicles due to a steering gear assembly nut that may not be properly tightened.
2 products
NHTSA•MODERATERockford Fosgate Amplifier KitsRockford is recalling four amplifier kit models due to a 150-amp fuse defect that poses a fire risk.
NHTSA•MODERATERicon S-Series and K-Series Wheelchair LiftsRicon is recalling S-Series and K-Series wheelchair lifts because a faulty electrical contactor may cause the lift to move unexpectedly.
FDA•MODERATEMethylergonovine Maleate TabletsMajor Pharmaceuticals is recalling 0.2 mg Methylergonovine Maleate Tablets due to subpotency.