FDA•MODERATE
Meclizine Hydrochloride Tablets 12.5 mg
American Health Packaging is recalling Meclizine Hydrochloride 12.5 mg tablets (NDC 60687-775-65 and 60687-775-11) due to failed tablet specifications.
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FDA•MODERATEeTRAX Needle System Starter Kit 12GCivco recalls eTRAX Needle System Starter Kit 12G (Part 667-149) due to sensor programming error causing incorrect needle tip position.
8 products
FDA•CRITICALCentrosFLO Hemodialysis CathetersMerit Medical recalls CentrosFLO Hemodialysis Catheters over sheath introducer defect that may cause hemorrhage and other serious complications.
5 products
FDA•CRITICALBaxter Volara Ventilator Adapter ModuleBaxter is issuing a correction for the Volara Respiratory Therapy system adapter module to prevent oxygen desaturation and lung injury.
FDA•CRITICALSpray Dried Dairy PowderLone Star Dairy Products is recalling Spray Dried Dairy Powder (25 kg bags, 1 metric ton totes) due to Salmonella contamination.
FDA•MODERATEPrazosin Hydrochloride Capsules 1mgAppco Pharma recalls Prazosin HCl 1mg capsules over nitrosamine impurity (NNP) above acceptable limits.
3 products
FDA•MODERATEK.C. Pharmaceuticals: Multiple Eye DropsK.C. Pharmaceuticals recalls multiple brands of sterile eye drops over sterility concerns.
15 products
FDA•CRITICALAbiomed Impella Purge CassetteAbiomed is recalling Generation 1 purge cassettes due to an increased risk of purge leaks.
2 products
FDA•MODERATEBromfenac Ophthalmic Solution 0.07%Alembic Pharmaceuticals is recalling Bromfenac Ophthalmic Solution 0.07% (NDC 62332-583-03) due to failed impurities and degradation specifications.
FDA•MODERATEJFE FRANCHISING: 7 productsJFE recalls Dumpling Party Trays and Loaded Dumpling Vegetable products over possible glass contamination.
7 products
FDA•MODERATETramadol Hydrochloride Tablets 50 mgAmneal is recalling 500-count bottles of Tramadol Hydrochloride 50 mg tablets due to an impurity found during stability testing.
FDA•MODERATECurosurf (poractant alfa) 240 mg Intratracheal SuspensionChiesi USA is recalling Curosurf 240 mg intratracheal suspension vials (NDC 10122-510-03) due to lack of sterility assurance.
FDA•MODERATESynthes VOLT Locking Screw TapSynthes recalls VOLT Locking and Cortical Screw Taps due to incorrect thread from a lot swap.
2 products
FDA•MODERATEOlympus SOLTIVE Laser SystemOlympus recalls SOLTIVE laser systems (TFL-SLS, TFL-PLS) due to power supply defect that may cause inoperability and smoke.
2 products
FDA•MODERATEEinstein Bros Bagels Honey Almond Double-Whipped ShmearEinstein Bros Bagels Honey Almond Double-Whipped Shmear recalled due to undeclared almond allergen.
FDA•MODERATEVital Nutrients Aller-CVital Nutrients Aller-C is recalled due to undeclared egg, soy, and hazelnut allergens.
CPSC•4our Kiddies Furniture Tip Restraint Kits4our Kiddies furniture tip restraint kits are recalled because the plastic components can break, posing tip-over and entrapment hazards.
CPSC•DuraTrac Stainless Steel Gas ConnectorsDuraTrac is recalling stainless steel gas connectors due to a manufacturing defect that poses a fire hazard from potential gas leaks.
CPSC•AirClub Convertible BassinetsAirClub convertible bassinets are recalled due to a fall hazard caused by a defective attachment mechanism that violates federal safety standards.
CPSC•MPINOI Adult Portable Bed RailsMPINOI adult portable bed rails are recalled due to a serious entrapment and asphyxiation hazard that violates federal safety standards.
CPSC•Nexgrill Metal Wire Bristle Grill BrushesNexgrill is recalling metal wire bristle grill brushes due to an ingestion hazard.
CPSC•GLMZZ Fidget Magnet Ball ToysGLMZZ Fidget Magnet Ball Toys are recalled due to a serious ingestion hazard that violates federal toy safety standards.
CPSC•FUNTOK Ride-On TrucksFUNTOK 24V 2-seater ride-on trucks (model DLS-K03) are recalled due to fire and burn hazards from an overheating circuit board.
CPSC•Sunnyyes LED Mini LightsSunnyyes LED mini lights are recalled due to a serious battery ingestion hazard that can cause internal chemical burns and death.
CPSC•CCCEI Power StripsCCCEI power strips are recalled due to a fire hazard caused by a lack of overcurrent protection.
CPSC•Petzl Nomic and Ergonomic Ice Climbing AxesPetzl is recalling Nomic and Ergonomic ice climbing axes due to a shaft breakage hazard that poses a risk of serious injury or death.
CPSC•DIY Sauna Heater KitsDIY Sauna Heater Kits are being recalled due to an overheating issue that poses a fire hazard and risk of serious injury or death.
CPSC•Vive Health Adult Portable Bed RailsVive Health is recalling adult portable bed rails due to entrapment and asphyxiation hazards that have resulted in two deaths.
FDA•MODERATESevillo Fine Foods Slow Roasted Diced TomatoesSevillo Fine Foods is recalling 24 lb boxes of frozen Slow Roasted Diced Tomatoes (SKU 900) due to potential metal fragment contamination.
2 products
FDA•MODERATEOctreotide Acetate Injectable Suspension 20 mgTeva recalls Octreotide Acetate 20 mg vials over sterility assurance concerns.
6 products
FDA•MODERATEArtoura Breast Tissue ExpandersA recall was issued for Artoura Breast Tissue Expanders due to infusion sets that may contain dull or blunt needle tips.
7 products
FDA•MODERATEPhilips Allura Xper FD10/FD20 Wired Foot SwitchPhilips recalls Allura Xper FD10/FD20 systems over wired foot switch failure causing intermittent X-ray imaging.
22 products
FDA•MODERATEBD Kiestra ReadABD Kiestra ReadA is recalled due to potential connectivity issues causing delays in plate retrieval after a system reboot.
FDA•CRITICALAbiomed Automated Impella ControllerAbiomed is recalling Automated Impella Controllers due to a potential delay in the "Purge System Blocked" alarm.
2 products
FDA•MODERATEMedline ENFit G-Tube ConnectorMedline recalls ENFit G-tube connectors in care/discharge kits over seal failure and leakage risk.
2 products
FDA•MODERATEEmbrace Drill TowerWaldemar Link recalls Embrace Drill Tower instruments over mixed-up article numbers in the surgical technique overview.
2 products
FDA•MODERATEJiffy Original Composite Polisher Cups (Coarse)Ultradent is recalling Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011, due to crumbling and breakage risk.
FDA•MODERATERefleXion X1 Radiotherapy System Model RXM1000RefleXion X1 Radiotherapy System Model RXM1000 recalled for software defect causing incorrect radiation dose delivery.
FDA•MODERATESterile Radiology Procedure Kits Model DYNDH1491BMedline is recalling Sterile Radiology Procedure Kits Model DYNDH1491B due to potential sterile pouch packaging breach.
FDA•MODERATEStryker CHROMOPHARE Softlit Ring Surgical LightStryker is recalling the CHROMOPHARE Softlit Ring Surgical Light System due to a potential ceiling cover support failure.
FDA•MODERATEParadise Ultrasound Renal Denervation CatheterReCor Medical is recalling the Paradise Ultrasound Renal Denervation Catheter (Model PRDS-068-02) as these units were intended to be scrapped.
3 products
FDA•MODERATEVue Motion V12 Imaging SystemPhilips Vue Motion V12 (1017979) may display image frames out of sequence during dynamic imaging runs.
FDA•MODERATEPuracol and Puracol Plus Collagen Wound DressingsMedline is recalling Puracol and Puracol Plus wound dressings due to elevated endotoxin levels that may cause severe inflammatory responses.
FDA•MODERATEAtellica CH Enzymatic Hemoglobin A1c AssaySiemens is recalling the Atellica CH A1c_E assay due to a risk of depressed results when used alongside the RCRP assay on the same analyzer.
FDA•MODERATEAmerican Laboratories: 3 productsAmerican Laboratories recalls pepsin powders (Full Strength, 1:10,000, 1:3000) due to potential Salmonella contamination.
3 products
FDA•CRITICALEspresso Malted Milk BallsNuts.com recalls Espresso Malted Milk Balls over undeclared wheat and soy allergens.
- Device RecallFDA•CRITICALPhilips Respironics Trilogy Evo Ventilator
Philips Respironics recalls Trilogy Evo ventilators over tidal volume discrepancy with non-pneumatic nebulizers.
4 products 
FDA•MODERATEBD Alaris System with Guardrails Suite MXBD Alaris System labeling lacks required TLS version specification for secure Wi-Fi communication with Point-of-Care Units.
FDA•MODERATENoromycin 300 LA Oxytetracycline InjectionMWI Animal Health is recalling Noromycin 300 LA oxytetracycline injection (NADA# 141-143) due to lack of assurance of sterility.
FDA•MODERATEWawa Beverage: 4 productsWawa recalls 4 flavored milk varieties (16 oz) over possible plastic contamination.
4 products