FDA•MODERATE
Xanax XR Alprazolam 3 mg Tablets
Viatris is recalling Xanax XR 3 mg tablets (NDC 58151-506-91) due to failed dissolution specifications.
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FDA•MODERATEB.R.A.H.M.S PlGF Plus KRYPTORBrahms recalls PlGF Plus KRYPTOR test (REF 859075N) due to QC underestimation risk causing false preeclampsia risk classification.
FDA•MODERATEVancomycin HCl 1.5g in 250mL Sodium Chloride InjectionFagron recalls Vancomycin HCl 1.5g/250mL injection due to sterility concern.
5 products
FDA•MODERATEGeri-Care Artificial Tears Lubricant Eye DropsGeri-Care Artificial Tears Lubricant Eye Drops (0.5 oz, NDC 68788-7266-0) recalled due to lack of sterility assurance.
FDA•CRITICALMedline Convenience Kits with Namic RA SyringesMedline recalls convenience kits with Namic RA syringes over risk of loose connection or disconnection during use.
25 products
FDA•MODERATEARTIS pheno and ARTIS Icono Biplane X-ray SystemSiemens is recalling ARTIS pheno and ARTIS Icono X-ray systems (Models 10849000, 11327600, 11328100, 11327700) due to erroneous dose display during patient exams.
FDA•MODERATESpacelabs Multi-parameter Command Module Model 91496Spacelabs is recalling Model 91496 Multi-parameter Command Module due to circuit board issue causing inaccurate cardiac output readings.
FDA•MODERATESee Luer Cap Set MPC-130Molded Products is recalling See Luer Cap Set MPC-130 due to threaded sleeve detachment risk.
CPSC•Coluans Christmas Light-Up RingsColuans Christmas Light-Up Rings (model SJP-50) are recalled due to a battery ingestion hazard that can cause serious injury or death.
CPSC•Beestech Spiral Children's Tower ToysBeestech spiral children's tower toys (Model Bee-210316-01) are recalled due to a choking hazard from small balls.
CPSC•Elenker Portable Bed RailsElenker portable bed rails are recalled due to a serious entrapment and asphyxiation hazard that violates federal safety standards.
CPSC•Universal Broadmoor Canopy Bed FramesSamson International is recalling Universal Broadmoor canopy bed frames due to a collapse hazard that poses a risk of impact and injury.
CPSC•Member's Mark Children's Pajama SetsMember's Mark children's pajama sets are recalled for violating federal flammability standards, posing a risk of burn injuries.
CPSC•Tuymec Minoxidil Hair Growth KitsTuymec Minoxidil Hair Growth Kits are recalled due to a lack of child-resistant packaging, posing a poisoning risk to young children.
CPSC•Gavoyeat Halloween Light-Up RingsGavoyeat Halloween Light-Up Rings (model 43398-68657) are recalled due to a battery ingestion hazard that can cause serious injury or death.
CPSC•Sangohe Adult Portable Bed RailsSangohe is recalling models 504E and 504Q adult portable bed rails due to serious entrapment and asphyxiation hazards.
FDA•MODERATEFresenius Kabi: Multiple Sale NDC Number InjectionsFresenius Kabi recalls 14 lots of Sodium Chloride and Dextrose Injections due to sterility concerns.
14 products
FDA•MODERATETornier HRS Max Tuberosity Body and Trial PartsTornier is recalling shoulder system components incorrectly labeled as HRS Max parts, as they are incompatible with the HRS Max system.
FDA•MODERATEMedline Anterior Hip Pack Biopsy ValveMedline is recalling Anterior Hip Packs containing Olympus biopsy valves over risk of rubber fragment detachment.
8 products
FDA•MODERATESIGNA Premier MR Scanner Magnet FittingsGE Healthcare is recalling SIGNA Premier MR scanners due to ferrous magnet fittings that could cause personnel injury during service.
FDA•MODERATEMedtronic MiniMed Insulin PumpsMedtronic MiniMed recalls all Paradigm, 600, and BLE 700 series insulin pumps over insulin delivery errors that can cause severe hypoglycemia or ketoacidosis.
14 products
FDA•MODERATEBurlington Medical Wrap ApronsBurlington Medical wrap aprons may lose shielding effectiveness over time.
13 products
FDA•MODERATEOXOID Microbact 12L Listeria Identification KitOxoid is recalling Microbact 12L Listeria Kit (MB1128A, Lot 4494873) due to risk of incorrect organism identification from ambiguous color reactions.
- Device RecallFDA•CRITICALPhilips Respironics Trilogy Evo O2 Ventilator
Philips Respironics recalls Trilogy Evo O2 ventilators (SW 1.05.15.00) over delayed obstruction alarm.
4 products 
FDA•MODERATECardinal Health Monoject Tuberculin Syringe 1 mLCardinal Health is recalling Monoject Tuberculin Syringes (Catalog 1180100777) that contain U-100 insulin syringes instead, risking dosing errors.
FDA•MODERATEMeclizine Hydrochloride Tablets 12.5 mgAmerican Health Packaging is recalling Meclizine Hydrochloride 12.5 mg tablets (NDC 60687-775-65 and 60687-775-11) due to failed tablet specifications.
FDA•CRITICALCentrosFLO Hemodialysis CathetersMerit Medical recalls CentrosFLO Hemodialysis Catheters over sheath introducer defect that may cause hemorrhage and other serious complications.
5 products
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•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
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•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•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•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•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•MODERATESterile Radiology Procedure Kits Model DYNDH1491BMedline is recalling Sterile Radiology Procedure Kits Model DYNDH1491B due to potential sterile pouch packaging breach.