CPSC•
TheKiddoSpace Children's Sensory Swings
TheKiddoSpace sensory swings are recalled due to a strangulation hazard posed by the fabric forming loops that can entangle a child.
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CPSC•TheKiddoSpace Montessori Egg Puzzle ToysTheKiddoSpace Montessori egg puzzle toys are recalled due to a choking and suffocation hazard for children under three.
CPSC•SumDirect LED Mini LightsSumDirect LED mini lights are recalled due to a serious battery ingestion hazard and lack of required safety warnings.
CPSC•TheKiddoSpace Children's Christmas Tree Play SetsTheKiddoSpace children's Christmas tree play sets are recalled due to lead exposure risk and failure to meet federal toy safety standards.
CPSC•Tubby Tots Fizzy Flask Bath Magic Bath Foam SetsTubby Tots Fizzy Flask bath foam sets (batch 082025) are recalled due to an impact hazard from pressure buildup in the containers.
CPSC•Trankerloop Baby Bath SeatsTrankerloop baby bath seats are recalled due to a drowning hazard, as they are unstable and can tip over during use.
CPSC•Magnetic Chess GamesMagnetic chess games are recalled due to a serious magnet ingestion hazard that can cause severe internal injuries or death in children.
CPSC•TheKiddoSpace Peg Doll Children's ToysTheKiddoSpace peg doll toys are recalled due to a choking hazard that violates the federal small parts ban for children under three.
CPSC•TheKiddoSpace Reusable Water BalloonsTheKiddoSpace is recalling reusable water balloons because the storage bag cord locks contain a regulated phthalate, violating a federal ban.
CPSC•Zelbuck Children's Chess GamesZelbuck children's chess games (model 999-9) are recalled due to a serious magnet ingestion hazard that can cause severe injury or death.
CPSC•Concord Bicycle HelmetsConcord 360 Degree Rechargeable Light-Up bike helmets are recalled for failing to meet federal safety standards, posing a head injury risk.
FDA•MODERATETeva Pharmaceuticals: multiple tabletsTeva recalls Metoprolol Succinate ER tablets (25-200 mg) over failed dissolution specs.
4 products
FDA•CRITICALImpella RP Flex with SmartAssistAbiomed recalls Impella RP Flex with SmartAssist due to sensor drift risk.
3 products
FDA•MODERATECobas Pro Integrated Solutions Analytical UnitsRoche is recalling Cobas Pro analytical units due to a software defect that can cause the system to report erroneous, repeated test results.
2 products
FDA•MODERATEGE Healthcare Centricity Universal ViewerGE Healthcare is recalling Centricity Universal Viewer software due to a risk of patient information and image mismatch.
FDA•CRITICALFish Ball: 3 Pieces Per PiecesKOI fish balls are being recalled because they contain undeclared wheat and sesame, which are allergens and pose a risk to people with wheat or sesame allergies.
3 products
FDA•MODERATEOctopus Nuvo Tissue StabilizerMedtronic is recalling Octopus Nuvo Tissue Stabilizer (TSMICS1) due to incorrect tubing assembly that may affect surgical tissue stabilization.
FDA•MODERATECampy CVA MediumRemel is recalling Campy CVA Medium (R01272) due to low recovery of Campylobacter Jejuni on identified lots.
FDA•MODERATEAgiliti Adapt PumpAgiliti is recalling the Adapt Pump (model 61600200) for a software failure that prevents the Microclimate Management function from restarting.
FDA•MODERATEPure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep ResetPure Solutions recalling 1 fl oz sleep formula bottles due to undeclared milk allergen from bovine colostrum.
FDA•MODERATEMedline Apheresis and Dialysis KitsMedline is recalling kits containing Tego Connectors due to potential silicone seal defects that may cause fluid leakage or therapy delays.
6 products
FDA•MODERATEEncore Medical Knee and Shoulder ImplantsEncore Medical is recalling EMPOWR 3D Knee and RSP Humeral Socket implants due to incorrect labeling.
3 products
FDA•MODERATEPIE PAK Trolley SystemEdermy is recalling PIE PAK trolley systems (models P2HC-A, P2HC-S, P2HC) due to a lack of required 510(k) clearance.
2 products
FDA•LOWEptifibatide Injection 75 mg/100 mLSlate Run Pharmaceuticals recalls Eptifibatide Injection 75 mg/100 mL vials (NDC 70436-027-80, 70436-163-80) due to incorrect dosing-route labeling.
FDA•MODERATEAmantadine HCl Capsules 100 mgAvKARE is recalling Amantadine HCl Capsules 100 mg (NDC 50268-069-15) nationwide due to failed dissolution specifications.
FDA•MODERATEAdbry (tralokinumab-ldrm) InjectionLEO Pharma is recalling Adbry (tralokinumab-ldrm) injection due to a lack of sterility assurance following the discovery of wool fiber.
FSIS•CRITICALBremer Italian Style MeatballsRosina recalls frozen Bremer Italian Style Meatballs over possible metal contamination.
FDA•MODERATEGerber Arrowroot BiscuitsGerber Arrowroot Biscuits (5.5 oz, UPC 015000005962) recalled for potential paper/plastic contamination in arrowroot flour.
CPSC•JJGoo LED Balloon LightsJJGoo LED balloon lights (Model MY1005E-Colorfu1-100) are recalled due to a serious battery ingestion and chemical burn hazard to children.
CPSC•Huaker Magnetic Balls and Rods SetsHuaker magnetic toy building sets (Model 20A-13) are recalled due to a serious choking hazard from small balls.
CPSC•Joly's 80% VinegarJoly's 80% Vinegar is recalled for missing mandatory safety labels, posing risks of poisoning and chemical burns.
CPSC•Prismatic 3D Prints Book NooksPrismatic 3D Prints is recalling Book Nooks because their spare coin batteries are easily accessible, posing a serious ingestion hazard.
CPSC•Vive Health Adult Portable Bed RailsVive Health is recalling models LVA1024 and LVA3031BLK bed rails due to a serious entrapment and asphyxiation risk.
CPSC•SAMIT Youth Multi-Purpose HelmetsSAMIT youth multi-purpose helmets are recalled for failing federal safety standards, posing a risk of serious head injury or death.
FDA•CRITICALKirkland Signature Mini BeignetsKirkland Signature Mini Beignets are recalled due to undeclared hazelnut, which poses a risk to consumers with allergies.
FDA•CRITICALUdenyca Pegfilgrastim-cbqv InjectionAccord BioPharma is recalling Udenyca injection due to improper storage temperature conditions.
FDA•MODERATEOxycodone Hydrochloride 5 mg TabletsAmerican Health Packaging is recalling Oxycodone 5 mg tablets due to defective blister card seals that may cause tablets to fall out.
FDA•MODERATECetrorelix Acetate Injection KitMeitheal Pharmaceuticals is recalling Cetrorelix Acetate injection kits due to missing or duplicated needles in the delivery system.
FDA•CRITICALOlympus High Flow Insufflation UnitOlympus is recalling the UHI-3 High Flow Insufflation Unit due to a software issue that may cause dangerous overpressure events.
3 products
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