CPSC•
Yeeluzan Pool Drain Covers
Yeeluzan pool drain covers are recalled due to entrapment and drowning hazards, as they violate federal safety standards.
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FDA•MODERATEHydroPeptide Clear Alliance SerumHydroPeptide Clear Alliance Serum recalled due to benzene contamination.
4 products
FDA•MODERATECinacalcet Hydrochloride Tablets 30 mgCipla recalls Cinacalcet HCl 30 mg tablets over N-Nitroso impurity above acceptable limit.
3 products
FDA•MODERATEExchange Select Honey Lemon Cough DropsExchange Select Honey Lemon Cough Drops recalled over quality concerns from FDA inspection.
15 products
FDA•MODERATERemel Yeastone BrothRemel is recalling Yeastone Broth due to the potential for incorrect antimicrobial susceptibility testing results.
FDA•MODERATELinkBio CORE WorkstationLinkBio CORE Workstation (87-9136) may display incorrect Planning Date on Start Case menu.
- Device RecallFDA•MODERATEPhilips AneurysmFlow Software
Philips is recalling AneurysmFlow software because the MAFA ratio provides unreliable prognostic data for aneurysm treatment decisions.
FDA•MODERATEArjo Tenor Mobile Patient LiftArjo Tenor patient lifts (Models KHA1000 US, KHA1010 US) recalled for actuator failure risk causing sudden arm drop.
CPSC•BISSELL Steam Shot OmniReach and Omni Steam CleanersBISSELL is recalling Steam Shot handheld steam cleaners due to a burn hazard from attachments that can detach and expel hot water or steam.
CPSC•Easymake Adult Portable Bed RailsEasymake adult portable bed rails are recalled due to an entrapment and asphyxiation hazard that violates federal safety standards.
CPSC•SCUBAPRO Monorail Weight PocketsSCUBAPRO is recalling Monorail Weight Pockets for BCDs because the D-ring handle can detach, posing a drowning hazard.
CPSC•Maitys Magnetic Drinkware CharmsMaitys magnetic drinkware charms are recalled due to an ingestion hazard from loose magnets that can cause serious injury or death.
CPSC•Iron-Containing Dietary SupplementsThe products lack required child-resistant packaging, posing a risk of serious injury or death from poisoning if swallowed by young children.
CPSC•Wybot Robotic Pool VacuumsWybotics is recalling Osprey 700 Max and S1 robotic pool vacuums due to battery overheating, posing burn and fire hazards.
CPSC•Silks Children's Loungewear SetsSilks children's loungewear sets are recalled for violating federal flammability standards, posing a serious burn risk to children.
CPSC•SNOOZ Breez 2-in-1 Smart Bedroom FansSNOOZ is recalling Breez 2-in-1 Smart Bedroom fans due to an overheating fire hazard caused by power connector corrosion.
FDA•MODERATELanreotide Injection 120 mg/0.5 mLCipla recalls Lanreotide Injection 120 mg/0.5 mL over sterility assurance concerns.
2 products
FDA•MODERATEOmnipaque (iohexol) Injection 350 mg/mLGE Healthcare recalls Omnipaque (iohexol) Injection 350 mg/mL due to particulate matter.
2 products
FDA•CRITICALBlaine Labs: multiple drugsBlaine Labs recalls multiple topical antiseptic/antifungal gels and creams due to Lysinibacillus fusiformis contamination.
9 products
FDA•MODERATEDivided Sunset Multi Collagen PeptidesDivided Sunset Multi Collagen Peptides are recalled for failing to declare egg and fish allergens on the product label.
FDA•MODERATEXanax XR Alprazolam 3 mg TabletsViatris is recalling Xanax XR 3 mg tablets (NDC 58151-506-91) due to failed dissolution specifications.
FDA•MODERATEIsotretinoin Capsules, USP, 40 mgTeva is recalling 40 mg Isotretinoin Capsules due to potency issues.
2 products
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.
FSIS•MODERATEGreat Value Dino Shaped Chicken NuggetsFSIS retracts alert for Great Value Dino Chicken Nuggets after follow-up testing finds no lead risk.
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•LOWSuper World Trading: 3 Heshan Mei Heong Yuen Food Pte NiesMei Heong Yuen roasted peanuts recalled over banned cyclamate sweetener.
3 products
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•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