FDA•MODERATE
Cetrorelix Acetate for Injection Kit 0.25 mg
Meitheal Pharmaceuticals recalls Cetrorelix Acetate injection kits (NDC 71288-558-90) due to missing or duplicated needles.
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FDA•MODERATERefleXion X1 Radiotherapy System Model RXM1000RefleXion X1 Radiotherapy System Model RXM1000 recalled for software defect causing incorrect radiation dose delivery.
FDA•MODERATEID NOW Influenza A & B 2 Test KitAbbott is recalling ID NOW Influenza A & B 2 test kits (Model 427-000) due to an increased rate of invalid test results.
NHTSA•MODERATEHarley-Davidson Sportster S Upper Triple ClampHarley-Davidson is recalling 2021–2026 Sportster S motorcycles due to upper triple clamp fracture risk.
FDA•MODERATEsmart & simple Turmeric PelletsSmartPak Equine is recalling smart & simple Turmeric Pellets due to elevated aflatoxin levels.
FDA•CRITICALLobster and Crab RavioliPerfect Pasta is recalling Lobster and Crab Ravioli due to undeclared shrimp, crab, lobster, pollock, whiting, and soy allergens.
NHTSA•MODERATEOshkosh NGDV Brake Pedal Mounting Pin and Retaining ClipOshkosh is recalling 2025–2026 NGDV vehicles; brake pedal mounting pin and retaining clip may be missing, risking brake failure.
FDA•MODERATEValley Springs 100% Natural Bottled WaterValley Springs is recalling 100% Natural Bottled Water (1 Gal) due to insanitary bottling conditions.
4 products
FDA•MODERATEArtelon FlexBand Dynamic MatrixInternational Life Sciences is recalling the Artelon FlexBand Dynamic Matrix due to failure to meet bacterial endotoxin testing requirements.
3 products
FDA•CRITICALTRUE METRIX Blood Glucose Meter Owner's BookletsTrividia Health is recalling TRUE METRIX meter manuals due to inadequate instructions for addressing the E-5 error code.
7 products
FDA•MODERATEBD Kiestra ReadABD Kiestra ReadA modules may experience connectivity issues after a reboot, potentially delaying plate retrieval.
FDA•LOWCardiosave Battery Charging StationDatascope is recalling the Cardiosave Battery Charging Station due to a design flaw in the left bay that prevents proper battery charging.
FDA•MODERATEHitachi Proton Beam Therapy SystemHitachi is recalling its Proton Beam Therapy System due to a software error that may cause inaccurate patient positioning during treatment.
2 products
NHTSA•MODERATEMercedes-Benz Metris Air Bag Control UnitMercedes-Benz Metris (2020, 2022–2023) air bag control units may fail to deploy due to water accumulation.
NHTSA•MODERATEHyundai IONIQ 5 and IONIQ 9 High Voltage BatteryHyundai is recalling 2025–2026 IONIQ 5 and 2026 IONIQ 9 vehicles over high voltage battery short-circuit fire risk.
NHTSA•CRITICALMercedes-Benz EQB High Voltage BatteryMercedes-Benz is recalling 2022–2024 EQB vehicles over high voltage battery fire risk while parked or driving.
NHTSA•MODERATEHyundai Kona Steering Knuckle AssemblyHyundai is recalling 2026 Kona vehicles with defective front steering knuckles that may crack, causing loss of steering control.
NHTSA•MODERATEVolvo S60L Door LatchVolvo is recalling 2017 S60L vehicles with defective door latches that may open unexpectedly.
NHTSA•MODERATEAltec Digger Derrick and AM Series Aerial Device Power Distribution ModuleAltec is recalling 2021–2025 Digger Derrick and AM Series Aerial Device vehicles; engine may start unexpectedly due to missing diode in power distribution module.
NHTSA•MODERATEToyo Open Country A/T III TireToyo is recalling Open Country A/T III tires (265/70R18, 265/60R20) due to tread separation risk.
FDA•MODERATETippy Toes Apple Pear Banana Baby FoodTippy Toes Apple Pear Banana baby food is recalled due to potential patulin contamination.
FDA•MODERATEThiamine HCl InjectionFagron Sterile Services is recalling Thiamine HCl 500 mg injection due to a lack of assurance of sterility.
5 products
FDA•MODERATECampy CVA MediumRemel is recalling Campy CVA Medium (R01272) due to low recovery of Campylobacter Jejuni on identified lots.
NHTSA•MODERATEJaguar I-PACE High Voltage BatteryJaguar is recalling 2020–2021 I-PACE vehicles; high voltage battery may overheat and catch fire.
FDA•MODERATESTA Liatest D-Di KitDiagnostica Stago is recalling the STA Liatest D-Di kit due to a positive bias that may cause inaccurate D-Dimer test results.
2 products
FDA•MODERATEDexamethasone Sodium Phosphate Injection, USP 100 mg/10 mLSomerset Therapeutics is recalling Dexamethasone Sodium Phosphate Injection (NDC 70069-025-10/01) due to out-of-specification impurities at expiry.
FDA•MODERATESTA Liatest Free Protein SDiagnostica Stago is recalling STA Liatest Free Protein S kits due to the risk of inaccurate test results for normal patient plasma levels.
NHTSA•MODERATEFreightliner Business Class M2 Steering GearboxFontaine Modification is recalling 2024–2025 Freightliner Business Class M2 vehicles over insufficient steering gearbox oil that may cause steering difficulty.
NHTSA•MODERATEMercedes Benz Tourrider Transit Bus Door Control ValveDaimler Coaches is recalling 2026 Mercedes Benz Tourrider transit buses with defective door control valves that may prevent door opening.
NHTSA•MODERATEEmber 2026 E-Series and Overland Series Travel TrailersEmber is recalling 2026 E-Series and Overland Series travel trailers with incorrect cargo capacity labels that may cause overloading.
NHTSA•MODERATEBMW 228i and M235i Gran Coupe Rear LightsBMW is recalling 2026 228i and M235i Gran Coupe vehicles with rear lights that may not function properly, increasing crash risk.
FDA•MODERATEReact Health PHOENIX 5L Oxygen ConcentratorReact Health PHOENIX 5L Oxygen Concentrator recalled due to devices not meeting quality specifications.
FDA•MODERATEIvenix Infusion System Large Volume PumpFresenius Kabi is recalling the Ivenix Infusion System LVP due to a risk of the cassette loading lever breaking during use.
FSIS•CRITICALMays Chemical Company Frozen Pork Boneless LoinsMays Chemical recalls 46,315 lbs of frozen pork boneless loins imported without U.S. reinspection; discard or return.
FDA•MODERATEPure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep ResetPure Solutions recalling 1 fl oz sleep formula bottles due to undeclared milk allergen from bovine colostrum.
FDA•MODERATECoco's Italian Market Cannoli Making KitCoco's Italian Market is recalling Cannoli Making Kits due to undeclared wheat and milk allergens.
2 products
FDA•CRITICALPrime Food Processing Dried Croaker FishPrime Food Processing is recalling Dried Croaker Fish due to the risk of botulism from uneviscerated fish.
FDA•LOWPitavastatin Tablets, 2 mgNorthstar Rx LLC is recalling Pitavastatin Tablets, 2 mg (NDC 72603-479-01) due to a foreign 1 mg tablet found in bottles.
FDA•MODERATEEquinoxe Ergo Modular Impactor HandleExactech is recalling the Equinoxe Ergo Modular Impactor Handle due to a missing cross-pin that may cause device failure.
2 products
FDA•MODERATEImactis CT-Navigation SystemGE Medical Systems is recalling Imactis CT-Navigation System (Models E85101LA, E85101LP) due to potential needle trajectory/tip position discordance.
FDA•MODERATEIBA Proton Therapy System PROTEUS 235IBA PROTEUS 235 proton therapy systems may fail to stop beam delivery if external gating device signal is lost, risking patient mistreatment.
NHTSA•MODERATEFord E-Transit High-Voltage Battery PackFord is recalling 2026 E-Transit vehicles over missing washers in the high-voltage battery pack that may cause electrical arcing and fire.
NHTSA•MODERATEFord Transit Engine CrossmemberFord is recalling 2023–2024 Transit vehicles over improperly secured engine crossmember that may cause loss of drive power or brake failure.
FDA•MODERATEPro Numb Tattoo Numbing SprayPro Numb is recalling 5% Lidocaine Tattoo Numbing Spray due to cGMP manufacturing deviations.
2 products
FDA•MODERATEB. Braun Winged Infusion SetsB. Braun is recalling 21GA Winged Infusion Sets (Model 7M2802) due to potential needle tip dullness or breakage.
3 products
FDA•MODERATEMICS3 Angled Sagittal Saw AttachmentHowmedica Osteonics is recalling MICS3 Angled Sagittal Saw Attachments because external screws may loosen and detach during use.
NHTSA•MODERATEChrysler Trailer Tow ModuleChrysler is recalling 2024–2026 Jeep Wagoneer S and Ram pickup/cab chassis vehicles over trailer tow module defects causing brake light and brake failure.
- Equipment RecallNHTSA•MODERATEMopar Tow Trailer Module
Chrysler is recalling Mopar tow trailer modules that may cause trailer lights and brakes to fail, increasing crash risk.
NHTSA•MODERATEPierce 2025 Velocity/Saber/Impel/Enforcer/Arrow XT Steering Linkage ArmPierce is recalling 2025 Velocity, Saber, Impel, Enforcer, and Arrow XT vehicles due to steering linkage arm detachment risk.
FDA•MODERATEOn-X Mitral Heart Valve with Conform-X Sewing RingOn-X is recalling Model ONXMC-25/33 Mitral Heart Valve due to incomplete testing before distribution.