CPSC•
Trek and Electra Electric Bicycle Rear Wheel Bolts
Hyena is recalling rear wheel bolts on 2026 Trek FX+ and Electra Townie Go! e-bikes sold before October 2025 due to fall hazard from wheel separation.
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CPSC•Viofairy Hair Growth Serum BottlesViofairy Hair Growth Serum (5% minoxidil) recalled for non-child-resistant packaging; risk of serious injury or death if swallowed by children.
CPSC•Sefudun 5% Minoxidil Hair Growth Serum KitSefudun 5% Minoxidil Hair Growth Serum Kit lacks child-resistant packaging, risking serious injury or death if ingested by children.
FDA•MODERATEPreema Bright Red and Orange Food Colour PowderPreema Bright Red and Orange Food Colour Powder recalled for banned carmoisine and undeclared FD&C Yellow 5 and Red 40.
2 products
FDA•MODERATEMetoprolol Succinate Extended-Release TabletsTeva is recalling Metoprolol Succinate Extended-Release Tablets due to failed dissolution specifications.
4 products
FDA•MODERATEOlympus Single Use Biopsy ValveOlympus is recalling the MAJ-210 single use biopsy valve due to the risk of rubber fragments detaching during use.
2 products
FDA•MODERATEParadise Ultrasound Renal Denervation CatheterReCor Medical is recalling the Paradise Ultrasound Renal Denervation Catheter (Model PRDS-068-02) as these units were not for human use.
3 products- Device RecallFDA•MODERATEB. Braun Cesk Northside Anesthesia Tray
B. Braun is recalling the Cesk Northside Anesthesia Tray (Model 555076) due to potential cracking of the included adhesive tubing.
8 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•MODERATEMedline Medcrest Surgical GownsMedline is recalling Medcrest surgical gowns due to a risk of fabric delamination during laundering, which may lead to infection.
3 products
FDA•MODERATEFrozen Half Shell OystersKhee Trading is recalling frozen half shell oysters due to potential Norovirus contamination.
FDA•MODERATEDiclofenac Sodium Topical Gel 3%Taro Pharmaceuticals is recalling Diclofenac Sodium Topical Gel 3% (100 g) due to viscosity specification failure.
FDA•MODERATEBD 10mL Non-Sterile Luer-Lok SyringeBD is recalling 10mL non-sterile Luer-Lok syringes (catalog 301029) due to incorrect Luer Slip syringes mixed into batches.
FDA•MODERATELutronic CLARITY II Laser SystemLutronic is recalling CLARITY II Laser System (Model 1110200210) due to sparking and burn hazard.
FDA•MODERATEKeto-C Antiseptic WipesStratford Care USA is recalling Keto-C Antiseptic Wipes (50ct) due to misbranding; product contains non-medicated otic flush instead of labeled antiseptic.
36 products
FDA•MODERATERepackaged M&Ms Peanut CandiesBeacon Promotions is recalling 1.3 oz repackaged M&Ms Peanut candies due to undeclared milk, soy, and peanut allergens.
3 products
FDA•MODERATEGerber Arrowroot BiscuitsGerber Arrowroot Biscuits (5.5 oz, UPC 015000005962) recalled for potential paper/plastic contamination in arrowroot flour.
FDA•MODERATEAsteria Health Testosterone Sterile PelletsAsteria Health is recalling 100 mg testosterone pellets due to potential metal particulate contamination.
25 products
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.
FDA•MODERATESodium Iodide (I-131) Therapeutic Oral SolutionRadnostix is recalling Sodium Iodide (I-131) Therapeutic Oral Solution due to the presence of particulate matter.
FDA•MODERATEPhilips Azurion 7 M12 SystemPhilips is recalling Azurion 7 M12 systems due to a risk of unexpected table movement when the Reset Geometry button is pressed.
8 products
FDA•MODERATETops GOLD PicklesMangalm LLC is recalling Tops GOLD pickle products due to potential erucic acid contamination from mustard oil.
6 products
FDA•MODERATEI.T.S. Headless Compression Screw SystemI.T.S. is recalling its Headless Compression Screw System due to updated MRI safety testing showing higher temperature risks.
24 products
FDA•MODERATEDatascope CS300 IABPDatascope is updating the IFU for CS300 IABP software version C.01 to correct battery runtime and cycle specifications.
2 products
FDA•MODERATERed Button Movie House PopcornLee's Commissary is recalling Red Button Movie House Popcorn due to potential foreign material contamination.
CPSC•Iristar Minoxidil Spray BottlesIristar Minoxidil Spray Bottles lack required child-resistant packaging, posing poisoning risk to children.
CPSC•Magellan Odyssey Rocker ChairsMagellan Odyssey Rocker Chairs (date codes 07/2025–08/2025) recalled due to breaking legs and fall hazards.
CPSC•Based Online Fidget Magnet Ball ToysBased Online is recalling Fidget Magnet Ball Toy Sets (4-pack, ~1.24" diameter) sold on Amazon Feb–Oct 2025 due to ingestion hazard from loose high-powered magnets.
CPSC•Cumbor Retractable Safety GatesCumbor retractable safety gates (Model S5V2) recalled due to entrapment risk from gaps between gate and floor.
CPSC•Matrix Retail and Vision TreadmillsJohnson Health Tech recalls Matrix and Vision treadmills (12 models, 2007–2024) due to loose power cord fire hazard; free replacement cord available.
CPSC•Angry Orange Enzyme Stain RemoverThrasio recalls Angry Orange Enzyme Stain Removers (24-oz, 32-oz, 1-gal) over possible Pseudomonas aeruginosa contamination.
CPSC•Mikario Trading 5-in-1 Convertible Baby GymMikario Trading's 5-in-1 baby gym (Item No. CBPBG-PIN) sold on TikTok Shop poses suffocation risk due to obstructive floor mats.
CPSC•Gagaku Children's Ice Cream Toy PlaysetGagaku ice cream toy playset (Model KABI-0176 G062401IC) recalled for detachable high-powered magnets posing serious ingestion hazard to children.
CPSC•Vndueey Magnetic Men Toy SetsVndueey Magnetic Men toy sets recalled for loose magnets posing serious ingestion hazard to children.
CPSC•Yetonamr Pull String Teething ToyYetonamr Pull String Teething Toy (Model 688-59) recalled for choking hazard from undersized silicone strings.
CPSC•Topkay Torch LightersTopkay Torch Lighters sold on Amazon lack child-resistant mechanisms, posing fire and burn hazards.
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.
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•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•MODERATEEVO+ Visian Toric Implantable Collamer Lens (TICL)Staar Surgical is recalling EVO+ Visian Toric ICL Model VTICM5 due to incorrect length labeling (12.1 mm labeled vs. 12.6 mm actual) causing excessive vault and potential angle closure.
FDA•MODERATEPhysio-Control Infant/Child Defibrillator ElectrodesPhysio-Control is recalling infant/child defibrillator electrodes due to a risk of delamination that may prevent proper therapy delivery.
2 products
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•MODERATEAdapt Pump Model 61600200Agiliti is recalling Adapt Pump Model 61600200 due to Microclimate Management function failure after Autofirm use.
FDA•MODERATECrunchy Caramel Dark ChocolateGarcia Nevett is recalling Crunchy Caramel dark chocolate bars due to an undeclared milk allergen.
FDA•MODERATEMed Nap BZK Antiseptic TowelettesAcme United is recalling Med Nap BZK Antiseptic Towelettes (NDC 0924-0246-01) due to CGMP deviations.
22 products
FDA•MODERATEGEM Premier 5000 PAKInstrumentation Laboratory is recalling GEM Premier 5000 PAK cartridges due to errors that may cause ejection and delay patient results.
20 products
FDA•MODERATECobas Pro Integrated Solutions Analytical UnitsRoche is recalling Cobas Pro integrated solutions due to a software defect causing the system to report erroneous, repeated lab results.
2 products
FDA•MODERATEAtellica CH Urine Albumin TestSiemens is recalling Atellica CH Urine Albumin tests (Material 11537225) due to falsely depressed results in high-concentration samples.
FDA•MODERATERoasted Tomato and Parmesan Focaccia BreadBakkavor is recalling various roasted tomato and parmesan focaccia breads due to potential metal fragment contamination.
3 products
FDA•MODERATEVegetarian Chicken Flavor RamenPalmetto Gourmet Foods is recalling Vegetarian Chicken Flavor Ramen due to undeclared Yellow #5.
2 products