FDA•MODERATE
Inspire Respiratory Sensing Lead
Inspire is recalling its Respiratory Sensing Lead (Model 4340) due to incorrect Use By Dates that may lead to premature revision surgery.
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FDA•MODERATEAdndale Magnesium Glycinate GummiesAdndale Magnesium Glycinate Gummies are being recalled due to the presence of undeclared melatonin.
FDA•MODERATEBD Connecta Luer-Lok StopcockBD is recalling Connecta Luer-Lok stopcocks due to a potential connection failure at Port C when using plastic luer-lok syringes.
FDA•MODERATESplashwire Hydrophilic Guide WireMerit Medical is recalling various Splashwire Hydrophilic Guide Wire models due to unsealed pouches that may compromise device sterility.
2 products
FDA•MODERATEBuprenorphine HCl InjectionPar Health is recalling Buprenorphine HCl Injection due to crystallization identified as Buprenorphine free base.
FDA•MODERATETriathlon Universal Baseplate Size 3/4Stryker recalls Triathlon Universal Baseplates due to size mislabeling in packaging.
2 products
FDA•MODERATEMedline Red Rubber Latex Urethral CathetersMedline recalls Red Rubber Latex Urethral Catheters (REF DYND13508–DYND13522, DYND13614/16) over surface, connector, and diameter defects.
34 products
FDA•MODERATEGiraffe OmniBed Canopy SoffitGE HealthCare recalls Giraffe OmniBed incubator/warmer over canopy soffit fastener risk that could injure patients.
3 products
FDA•MODERATEConMed AirSeal 5 mm Access PortConMed recalls AirSeal 5 mm Access Port (iASB5-150) over overpressure alert risk.
11 products- Device RecallFDA•MODERATESTAAR ICL Calculation Software
Staar Surgical is recalling Version 8.00 of its ICL Calculation Software due to a coding error affecting toric lens orientation diagrams.
2 products 
CPSC•Arrogantf Spa Drain CoversArrogantf spa drain covers are recalled due to entrapment and drowning hazards, as they violate federal safety standards.
FDA•MODERATEPhilips MultiDiagnost Eleva Hand SwitchPhilips recalls MultiDiagnost Eleva systems over hand switch that may not release, risking unintended radiation.
3 products
FDA•MODERATENutrisystem Chocolate CheesecakeNutrisystem is recalling Chocolate Cheesecake 2 oz packages due to an undeclared soy allergen.
FDA•MODERATEGreat Value Hawaiian Roll 4pkGreat Value Hawaiian Roll 4pk recalled over oily substance on food-contact packaging; product never reached store shelves.
FDA•MODERATERitmed Neurological SpongesAMD Medicom recalls Ritmed Neurological Sponges due to elevated endotoxin risk; full REF list on FDA page.
2 products
FDA•MODERATEdirectCHECK ACT-LR Whole Blood Quality ControlAccriva Diagnostics is recalling directCHECK ACT-LR whole blood quality control, level 2, due to incorrect performance range labeling.
FDA•MODERATEMID DOLCIARIA SRL: 2 Via Casalini BelpassosMID DOLCIARIA recalls Cannoli Siciliani and Crunchy Cannoli Gluten Free over unapproved colors E140/E141.
2 products
FDA•MODERATETrigen Proximal Straight Humeral NailSmith & Nephew is recalling the Trigen Proximal Straight Humeral Nail due to a manufacturing error that may cause surgical delays or revision.
FDA•MODERATEAripiprazole 30 mg TabletsAjanta Pharma is recalling Aripiprazole 30 mg tablets due to a mix-up with Voriconazole 50 mg tablets.
FDA•MODERATEMedtronic O-arm O2 Imaging SystemMedtronic is recalling the O-arm O2 Imaging System due to a firmware anomaly that may cause image artifacts during clinical use.
FDA•MODERATEHarmonyAIR A-Series Surgical Lighting SystemHarmonyAIR A-Series surgical lights recalled: intensity buttons may detach.
2 products
FDA•MODERATEHarmonyAIR A-Series Surgical Lighting SystemSteris is recalling HarmonyAIR A-Series Surgical Lighting Systems due to a risk of paint delamination on the light heads.
FDA•MODERATEPepperoni Rolls 5 ozPepperoni Rolls recalled for undeclared milk allergen and improper refrigeration; 5 oz packages.
FDA•MODERATEDabur India: Multiple Made In India ProductsDabur India recalls 14 OTC topical products over CGMP deviations.
14 products
FDA•MODERATEChlorthalidone 25 mg TabletsChlorthalidone 25 mg tablets are being recalled due to failed dissolution specifications.
FDA•LOWFocalin XR 5 mg CapsulesSandoz is recalling Focalin XR 5 mg capsules due to missing or incorrect lot numbers and expiration dates on the product labels.
FDA•MODERATEAlyacen 7/7/7 TabletsGlenmark is recalling Alyacen 7/7/7 tablets due to out-of-specification results for total impurities.
FDA•MODERATEVasopressin 2 Units/2 mL SyringesIntegraDose is recalling Vasopressin 2 Units/2 mL syringes due to subpotency, which may cause the drug to be ineffective.
FDA•MODERATEPAI: Multiple Kerr Insta-char In An ProductsVistaPharm recalls Kerr Insta-Char activated charcoal (25g/50g) for failing OTC monograph requirements.
4 products
FDA•MODERATEMedline EBSI KitMedline recalls EBSI Kit (EBSI1534) due to cracked butyrate tubing and recalled MASTISOL adhesive.
42 products
CPSC•Hasuit 7-Drawer DressersHasuit 7-Drawer Dressers are recalled due to tip-over and entrapment hazards that violate federal safety standards.
CPSC•Black Sheep Fam Kids' PajamasBlack Sheep Fam Kids' pajamas are recalled for violating federal flammability standards, posing a risk of serious burn injuries or death.
CPSC•Arctic Zone Titan Pro CoolersArctic Zone Titan Pro coolers are recalled due to a choking hazard from a detachable latch magnet.
CPSC•Kidisle Single-Serve CoffeemakersKidisle single-serve coffeemakers (Model KC101B) are recalled due to a burn hazard from unexpected hot liquid or steam release.
CPSC•Hopelight Adult Portable Bed RailsHopelight model F311 adult portable bed rails are recalled due to serious entrapment and asphyxiation hazards.
CPSC•Houoto Pool Drain CoversHouoto 642-2150V pool drain covers are recalled for violating federal safety standards, posing entrapment and drowning hazards.
CPSC•Kitchen HQ Thermal Insulated BowlsKitchen HQ thermal insulated bowls are being recalled due to a fire hazard when used in a microwave.
CPSC•Sloosh Dive SticksJoyin is recalling Sloosh dive sticks (model 40041) due to an impalement hazard that violates the federal dive sticks ban.
CPSC•Kawasaki Teryx4 H2 and Teryx5 H2 Off-Road VehiclesKawasaki is recalling 2026 Teryx4 H2 and Teryx5 H2 off-road vehicles due to a drive converter sheave failure that poses impact and injury risks.
CPSC•LiKee Pull String Teething ToysLiKee Pull String teething toys (Model LK-FDWJ) are recalled due to a choking hazard that violates federal toy safety standards.
CPSC•Merkury Innovations Hot + Cool FansMerkury Innovations is recalling model MI-DHC02 Hot + Cool fans due to an overheating fire hazard that poses a risk of serious injury or death.
CPSC•Nimood Adult Portable Bed RailsNimood is recalling C3 Pro, C4 Pro, C5 Pro, and C5 Pro 2.0 adult portable bed rails due to serious entrapment and asphyxiation hazards.
CPSC•Childcraft Furniture Tip Restraint KitsSchool Specialty is recalling tip restraint kits included with Childcraft furniture due to tip-over and entrapment hazards.
CPSC•Timechee Changing Table DressersTimechee changing table dressers are recalled due to tip-over and entrapment hazards that violate federal safety standards.
CPSC•Yamaha Drive2 Electric Fleet Golf CarsYamaha is recalling 2021-2022 Drive2 Electric Fleet Golf Cars due to a brake cable defect that poses a crash and injury risk.
CPSC•Yamaha UMAX Bistro and Bistro Deluxe VehiclesYamaha is recalling 2019–2025 UMAX Bistro and Bistro Deluxe vehicles due to an inaccurate weight capacity label that poses an injury hazard.
FDA•MODERATENiacin Extended-Release Tablets 1,000 mgGolden State Medical Supply is recalling Niacin Extended-Release Tablets, 1,000 mg, due to failure to meet dissolution specifications.
2 products
FDA•MODERATEFresh Roast Systems ColorTrack InstrumentFresh Roast Systems is recalling the ColorTrack instrument (Model BENCH R-100) due to a potential laser safety hazard.
FDA•MODERATEHalyard Pain PackAVID Medical recalls Halyard Pain Pack kits (AMPK48-01) over possible lack of sterilization.
4 products
FDA•MODERATEMOSAIQ Oncology Information SystemElekta is recalling the MOSAIQ Oncology Information System due to a software error that may prevent the loading of baseline shift plans.