FDA•CRITICAL
Olympus High Flow Insufflation Unit
Olympus is recalling the UHI-3 High Flow Insufflation Unit due to a software issue that may cause dangerous overpressure events.
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FDA•MODERATELaerdal Compact Suction Unit 4 RTCALaerdal is recalling LCSU 4 RTCA suction units due to potential electromagnetic noise levels exceeding regulatory limits.
FDA•MODERATEMedline Surgical and Biopsy Convenience KitsMedline is recalling various surgical and biopsy convenience kits due to potential issues with the sterility assurance level.
62 products
FDA•MODERATEAuris Health MONARCH Platform Bronchoscopy SystemAuris Health is recalling MONARCH Platform Bronchoscopy systems due to a software issue that may cause unexpected robotic arm repositioning and contact with the patient.
FDA•MODERATEMOLLI 2 Surgical Marker SystemStryker is updating the MOLLI 2 System labeling due to the risk of magnetized surgical tools dislodging markers during tissue removal.
2 products
FDA•CRITICALRosabella Moringa Dietary Supplement CapsulesAmbrosia Brands is recalling Rosabella Moringa dietary supplement capsules due to potential Salmonella contamination.
CPSC•CheerKid Baby Bath SeatsCheerKid baby bath seats (Model BH-222) are recalled due to a drowning hazard, as they can tip over during use.
CPSC•Watkins Highlife Collection Spa Hydromassage Rotary JetsWatkins is recalling 6-fin hydromassage rotary jets in 2023–2025 Highlife Collection spas due to hair entanglement and drowning hazards.
CPSC•Beloems Adult Portable Bed RailsBeloems model BL-BR201 adult portable bed rails are recalled due to serious entrapment, asphyxiation, and laceration hazards.
CPSC•Fortemotus Adult Portable Bed RailsFortemotus adult portable bed rails (model USFTMTJAS008) are recalled due to entrapment, fall, and laceration hazards.
FDA•MODERATEThiamine HCl Injection 500 mg/100 mLFresenius Kabi recalls thiamine HCl 500 mg/100 mL IV bags over sterility concerns.
5 products
FDA•MODERATEMediHoney Gel DressingIntegra LifeSciences is recalling MediHoney Gel dressing models 31805 and 31815 due to a potential breach in the sterile packaging barrier.
3 products
CPSC•SOOWERY 6-Drawer DressersSOOWERY 6-Drawer Dressers are recalled due to tip-over and entrapment hazards that pose a risk of serious injury or death to children.
CPSC•LShome Photoelectric Smoke Detector Fire AlarmsLShome smoke detectors are recalled for failing to sound during a fire, posing a serious injury or death hazard.
CPSC•Aroeve Air PurifiersAroeve is recalling model MK04 air purifiers due to an overheating risk that poses fire and burn hazards.
FDA•MODERATETestosterone 100 mg Sterile PelletsAsteria Health recalls Testosterone 100 mg Sterile Pellets over possible metal contamination.
25 products
FDA•MODERATEDiclofenac Sodium Topical Gel 3%Taro Pharmaceuticals is recalling Diclofenac Sodium Topical Gel 3% (100 g) due to viscosity specification failure.
FDA•LOWDoxazosin Tablets, USP 4 mgUnichem is recalling Doxazosin Tablets 4 mg (NDC 29300-353-10) due to incorrect tablet imprinting that may cause medication errors.
FDA•MODERATETrazodone Hydrochloride 50 mg TabletsGranules Pharmaceuticals is recalling Trazodone Hydrochloride 50 mg tablets (NDC 70010-231-01) due to foreign tablets or capsules in bottles.
- Device RecallFDA•MODERATEPhilips Azurion 5 M20 and 7 M12 Systems
Philips recalls Azurion 5 M20 and 7 M12 systems over risk of unexpected table movement when Reset Geometry is pressed.
8 products 
FDA•MODERATEAlphatec Spine Lateral Navigation Disc Prep InstrumentsAlphatec Spine is recalling 10mm Osteotome navigation instruments due to a design flaw in the array connection geometry.
2 products
FDA•MODERATEPro Numb Tattoo Numbing SprayPro Numb Tattoo Numbing Spray recalled over cGMP deviations.
2 products
FDA•MODERATEHalyard Transport Bag Kit LIFE0080-01Halyard Transport Bag Kit LIFE0080-01 recalled due to Tyvek bag seal issue that may compromise sterility.
FDA•LOWStraumann WB Impression Post Closed TrayStraumann is recalling WB Impression Post Closed Tray kits (L 13mm) due to incorrect magenta impression caps instead of brown.
FDA•CRITICALTRUE METRIX Blood Glucose Meter InstructionsTrividia recalls TRUE METRIX meter instructions over inadequate E-5 error guidance.
7 products
CPSC•EnHomee 10-Drawer DressersEnHomee 10-Drawer Dressers are recalled due to tip-over and entrapment hazards that pose a risk of serious injury or death to children.
CPSC•Lancaster Table & Seating Outdoor Chairs and BarstoolsLancaster Table & Seating outdoor chairs and barstools are recalled due to a fall hazard caused by legs that can bend or break during use.
CPSC•Fixwal 7-Drawer DressersFixwal 7-drawer dressers are recalled due to tip-over and entrapment hazards that pose a risk of serious injury or death to children.
CPSC•PurSteam Elite and Mighty Lil SteamersAterian is recalling PurSteam Elite and Mighty Lil steamers due to a burn hazard from hot water expulsion.
CPSC•Cobelae Busy BooksCobelae Busy Books are recalled due to a choking hazard from detachable beads on the apple page.
CPSC•Furnulem 5-Drawer DressersFurnulem 5-drawer dressers (Model HK-DS-017-CL-5D-1-W) are recalled due to tip-over and entrapment hazards.
CPSC•Scepter B62 Fuel ContainersScepter B62 fuel containers are recalled for lacking flame mitigation devices and child-resistant spouts, posing fire and poisoning risks.
CPSC•Little Cow Co. 9 oz CandlesLittle Cow Co. 9 oz candles are being recalled due to fire, burn, and laceration hazards from glass jars that can crack or break during use.
CPSC•GM Gumili Wintergreen Essential OilGM Gumili Wintergreen Essential Oil is recalled for failing to meet child-resistant packaging requirements, posing a poisoning risk to children.
CPSC•YITA 16-Drawer DressersYITA is recalling five brands of 16-drawer dressers due to serious tip-over and entrapment hazards.
CPSC•Lotus Joy Sweet Birch Essential OilLotus Joy Sweet Birch Essential Oil is recalled due to a lack of child-resistant packaging, posing a poisoning risk to young children.
CPSC•Semfri Children's HelmetsSemfri children's helmets are recalled for failing to meet federal safety standards, posing a risk of serious head injury or death.
CPSC•Lola + The Boys Youth Hooded ClothingLola + The Boys is recalling five styles of youth hooded clothing due to a strangulation hazard posed by drawstrings.
CPSC•Kitosun Submersible LED LightsKitosun is recalling Submersible LED Lights due to a serious battery ingestion hazard to children.
CPSC•Organic Zing Birch Essential OilOrganic Zing Birch Essential Oil is recalled due to missing child-resistant packaging, posing a poisoning risk to young children.
FDA•MODERATEPhilips Brilliance iCT Gantry Rotor FastenersPhilips is recalling Brilliance iCT systems due to a risk of rotor parts becoming unsecured and potentially expelled during gantry rotation.
4 products
FDA•MODERATEOlympus Single Use 3-Lumen Sphincterotome VOlympus is recalling the Single Use 3-Lumen Sphincterotome V (Model KD-V411M-1520) due to a risk of deformation and performance loss.
30 products
FDA•MODERATEMaquet Venous Bubble SensorMaquet is recalling the Venous Bubble Sensor (Model 701055720) due to cable durability issues that may cause device errors.
FDA•MODERATEFDR Visionary Suite X-ray GeneratorFUJIFILM is recalling FDR Visionary Suite X-ray generators due to a risk of overheating and smoke caused by faulty electromagnetic contactors.
FDA•MODERATEBeacon Promotions: 3 productsBeacon Promotions recalls repackaged M&Ms candies due to undeclared milk, soy, and peanut allergens.
3 products
FDA•MODERATEVITEK 2 Gram-negative Susceptibility CardsBiomerieux is recalling 30+ VITEK 2 susceptibility cards due to potential quality control failures and false resistant test results.
2 products
FDA•MODERATEPrismaflex M100 SetVantive is recalling the Prismaflex M100 Set due to a potential dislodgement of the deaeration chamber from the control unit.
8 products
FDA•MODERATEEncore Medical EMPOWR Acetabular and Knee InsertsEncore Medical is recalling EMPOWR acetabular liners and knee inserts due to a packaging discrepancy that may cause surgical delays.
2 products
FDA•MODERATEBisoprolol Fumarate and Hydrochlorothiazide Tablets 2.5 mg/6.25 mgUnichem Pharmaceuticals recalls Bisoprolol/Hydrochlorothiazide 2.5/6.25 mg tablets (NDC 29300-187-01) due to N-Nitroso Bisoprolol impurity specification failure.
CPSC•Sunneday and Blue Bay Above-Ground PoolsSunneday and Blue Bay above-ground pools are recalled due to a drowning hazard created by compression straps that can act as footholds.