All Recalls

DonJoy IceMan Classic Cube recalled due to broken connector interrupting cold therapy.

Analemma is recalling 24 oz stainless-steel water bottles due to a risk of serious injury or death from glass liner breakage.

EEMB is recalling lithium coin batteries in non-child-resistant packaging, posing a serious ingestion and chemical burn hazard to children.

Favoto is recalling Model H-1 bicycle helmets because they fail to meet federal safety standards, posing a serious head injury risk.

Foubeaka and Geniuss multi-purpose helmets are recalled for failing to meet federal safety standards, posing a risk of serious head injury.

Natural Pigments is recalling Rublev Colours Gum Turpentine and Mineral Spirits due to missing child-resistant packaging and poisoning risks.

Justforjoyful Rainbow Wall Toy (model JJ1602) is recalled due to a choking hazard posed by the xylophone drumstick.

Svnntaa adult portable bed rails are recalled due to serious entrapment, asphyxiation, fall, and laceration hazards.

ZMC Group is recalling various light-up toys due to a risk of serious injury or death from accessible button cell batteries.

Lundberg Family Farms recalls White Jasmine Rice 32 oz over possible foreign material contamination.

Orthorebirth recalls BioCera Fibers bone void filler (REFs ORB-0320C-KC, ORB-0310C-KC, ORB-0304C-KC, ORB-0302C-KC, ORB-0305D-KC) for out-of-spec.

Medline is recalling Ancillary Pack-LF and Open Heart Anesthesia ICC-A kits due to potential issues with sterilization and packaging calibration.

Breckenridge Pharmaceutical is recalling Duloxetine 60mg capsules distributed nationwide due to the presence of an impurity above FDA limits.

Acella Pharmaceuticals is recalling Naproxen Oral Suspension, 125 mg/5mL, distributed nationwide due to lead and lithium contamination.

BioFire is recalling the Joint Infection (JI) Panel due to contamination that may cause false positive test results.

Mint Medical is recalling Mint Lesion software versions 3.4.0–3.9.5 due to a risk of data loss or incorrect patient information linking.

One Step 10A in vitro diagnostic test recalled for lack of FDA clearance.

BioFire is recalling the Spotfire Respiratory/Sore Throat Panel due to the risk of false negative results and control failures.

Katalyst Surgical recalls DEX Ophthalmic Tissue Forceps, model DVF4005-23, due to IFU corrective action.

John B. Sanfilippo recalls nut mixes over Salmonella risk.

Woodstock Organic Shelled Edamame recalled over possible metal pieces.

Teva is recalling Octreotide Acetate 30 mg injection kits due to a lack of assurance of sterility.

Rising Pharma is recalling Enalapril Maleate 20 mg tablets (NDC 64980-688-10) due to failed impurities test.

CareFusion is recalling BD PurPrep sterile solution due to a lack of assurance of sterility and potential product contamination.

Utz is recalling Zapp's and Dirty potato chips in several varieties for possible Salmonella contamination.

Fresenius recalls DELFLEX dialysis solution due to potential bag leaks compromising sterility.

Ajanta recalls Duloxetine 30 mg capsules over nitrosamine impurity above FDA limit.

Physio-Control is recalling various LIFEPAK defibrillators serviced without proper performance inspections, potentially delaying therapy.

Second Nature recalls Keto Crunch Smart Mix 10 oz pouches due to undeclared cashews, pistachios, and dried cherries.

Unichem is recalling 5 mg buspirone hydrochloride tablets due to subpotency, which may reduce the medication's effectiveness.

Spacelabs is recalling the Ultraview SL Command Module due to a manufacturing issue with the electrical leakage tester.

Centinel Spine recalls Prodisc C SK cervical disc implants due to labeling mix-up (5mm/6mm).

Cook recalls Centimeter Sizing Catheter (RPN N5.0-35-100-P-10S-PIG-CSC-20) over marker band cracking risk.

Boston Scientific recalls LUX-DX II Arrhythmia Detector (M302) with LATITUDE DRAGON US Server (6460) over missing PVC Burden and Bradyarrhythmia monitoring.

Erbe Medical recalls ERBEFLO CleverCap CO2 tubing/cap sets due to risk of water aspiration and respiratory failure.

Intuitive Surgical is recalling the USM arm sub-assembly for da Vinci X and Xi systems due to a risk of internal screw breakage.

Intuitive is recalling SureForm 30 Gray stapler reloads due to the risk of an incomplete staple line during surgical procedures.

Hepo adult portable bed rails are recalled due to serious entrapment, asphyxiation, fall, and laceration hazards.

Acer is recalling AES015 electric scooters due to a loose screw that can cause the front tube to collapse, posing a fall hazard.

Honda is recalling 2025-2026 off-road motorcycles (CRF250/450 series) due to a handlebar clamp defect that poses a crash hazard.

Malker is recalling bicycle light sets due to a battery ingestion hazard that can cause serious injury or death.

1-K Kerosene Heater Fuel containers are recalled due to missing flame mitigation devices and lack of child-resistant closures.

Earthtec pool drain covers are recalled due to entrapment and drowning hazards, as they violate federal safety standards.

Stephan Baby Boo Bunnie and Friends toys are recalled due to choking and laceration hazards from the toy's plastic cube breaking.

UHOMEPRO 5-drawer dressers are recalled due to tip-over and entrapment hazards that violate federal safety standards.

DGIVOVO US is recalling model C4012PLUS-1500C electric pressure washers due to shock and electrocution hazards from a missing GFCI.

Qumeney bicycle light sets (models BL-01 and BL-02) are recalled due to a battery ingestion hazard that can cause serious injury or death.

Thermos is recalling Stainless King food jars and bottles because the stoppers can forcefully eject, posing impact and laceration hazards.

The StrikeLock hoistway door locking device is recalled due to a risk of serious injury or death from fall hazards.

Segmart 4-Drawer Dressers are recalled due to tip-over and entrapment hazards, as they fail to meet mandatory safety standards.