All Recalls

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.

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.

Chrysler recalls 2023–2026 Ram 2500 pickups; powertrain software error may allow speed to exceed tire rating.

Chrysler recalls 2019–2023 Jeep Cherokee over power transfer unit failure risk.

GM is recalling 2026 Cadillac, Chevrolet, and GMC 4WD/AWD vehicles and certain 2015–2020 models due to a missing transfer case component that may cause wheel lockup.

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.

Micro Bird recalls 2023–2026 G5 and 2024 MB II school buses; drive belt pulley may damage oil lines and cause fire risk.

Micro Bird recalls 2023–2025 G5 transit buses; drive belt pulley may damage oil lines and cause fire risk.

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.

Tesla recalls Model 3, Y, S, X vehicles with delayed rearview camera image in reverse (software 2026.8.6).

Winnebago is recalling 2026–2027 Solis RVs; LP hose may be incorrectly routed over exhaust heat shield, risking fire.

Shyft is recalling 2025 Utilimaster Velocity vehicles with incorrect cargo capacity labels.

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.

2026 Toyota 4Runner recalled for incorrect load capacity label that may lead to improper loading.

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

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.

Mercedes-Benz is recalling 2024–2026 AMG GT, C-Class, E-Class, SL, CLE, and GLC vehicles; infotainment unit may reset and blank the instrument panel display.

Braun is recalling 2026 Ram ProMaster vehicles with rear bench seats missing two of four legs.

New Flyer is recalling 2022 XE40 transit buses with speedometers that may not illuminate with headlights on.

Mercedes-Benz recalls 2026 CLA 350 4MATIC and CLA 250+ front passenger seat belts that may remain locked and cannot extend.

Waymo recalls 5th and 6th Gen ADS software that may drive vehicles into standing water on high-speed roads.

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.