
NHTSA•MODERATE
Hyundai Elantra Hybrid Power Control Unit
Hyundai is recalling 2024-2026 Elantra Hybrid vehicles because the hybrid power control unit may overheat, increasing the risk of fire.

Hyundai is recalling 2024-2026 Elantra Hybrid vehicles because the hybrid power control unit may overheat, increasing the risk of fire.

Hyundai is recalling 2015-2016 Elantra and 2016 Elantra GT vehicles because the driver's air bag inflator may rupture during deployment.

Altec is recalling various aerial device vehicles because the emergency stop may fail to halt hydraulic functions, increasing injury risk.

Honda is recalling 2024-2025 Honda Prologue and 2024 Acura ZDX vehicles because the rearview camera may display a distorted or blank image.

BMW is recalling 2017-2018 C Evolution motorcycles due to a fire risk from potential corrosion in the DC/DC converter electrical connection.

GM is recalling 2025–2026 Cadillac, Chevrolet, and GMC vehicles with 24-inch wheels due to incorrect front wheel hub bolts that may loosen.

Integra LifeSciences is recalling the Codman CerebroFlo EVD Catheter due to out-of-specification endotoxin results.

BARD Dynamic Deca Steerable EP catheter recalled due to incomplete seals on sterile product.
26 products
Edwards Lifesciences is updating the labeling for the EVOQUE tricuspid delivery system to include a warning about potential functionality issues.

Hale Products is recalling Weldon UV800 display units (part numbers 610-00060-080-51, 610-00060-080-50, 610-00060-081, 610-00091) due to failure.

Hiab is recalling Waltco MDV series liftgates because broken deck pins may cause the platform to fall, posing an injury risk.

Lucid is recalling 2024-2025 Air vehicles due to a Gen 4 inverter defect that may cause a loss of drive power and increase crash risk.

Fly By Jing recalls Creamy Sesame Noodles over possible undeclared peanut allergen.

ZYMUTEST HIA IgG ELISA kit lot FD1265 distributed with outdated flyer containing incorrect positive control values.

Philips is recalling Azurion imaging systems due to potential loosening or breakage of Cable Hose Carrier bolts and plastic parts.

Quidel is recalling QuickVue Dipstick Strep A Test (REF 20108) due to risk of false positive results.

Stryker is recalling the FluidSmart Urology Tube Set (REF LL0006) due to the distribution of nonconforming products.

Hologic recalls Selenia Dimensions mammography systems over loose or broken internal bolts.
2 products
Piaggio is recalling 2026 Vespa GTV 310, Primavera 150, and Primavera 50 motorcycles (Officina 8 color) with missing rearview mirror warning labels.

Ford is recalling 2026 Escape and Lincoln Corsair vehicles because a faulty park module can cause the vehicle to roll away.

Ford is recalling 2021-2022 Bronco vehicles with Molded-In-Color hardtop roof panels that may detach while driving, creating a road hazard.

Land Rover is recalling 2026 Range Rover, Velar, and Sport vehicles (NHTSA 26V297000) because the seat belt chime may not activate.

Nova Bus is recalling 2019-2023 LFS transit buses because the driver's door window may be missing a required DOT code mark.

Ascend Laboratories is recalling 25 mg Metoprolol Succinate Extended-Release Tablets due to failed dissolution testing.

Dexcom recalls G7 CGM iOS App (v2.9.0–2.11.2) over glucose alert delays that may cause missed hypo/hyperglycemic events.
4 products
Endo USA recalls Buprenorphine Hydrochloride Injection 0.3mg/mL vials (NDC 42023-179-05) due to particulate matter contamination.

Diowave 250W Laser System recalled; software update needed to correct power output exceeding FDA-cleared 60W limit.

Jolife AB is recalling LUCAS 2, 3, and 3.1 chest compression systems due to missing service documentation.
2 products
Forest River recalls 2026 Prime Time Crusader trailers; waste tank vent may release sewer gas into cabin.

International is recalling 2026–2027 HV vehicles for delayed service brake release that increases crash risk.

Tenneco is recalling Beck/Arnley lower control arm and ball joint assemblies for 2018-2025 Subaru vehicles due to a steering loss risk.

Braun is recalling 2023-2026 Chrysler Pacifica vehicles because the wheelchair restraint retractor may fail to lock, increasing injury risk.

Oasis Tears PF eye drops (NDC 42126-6400-1) recalled due to lack of assurance of sterility.

Dakota Honey recalls Spreadable Spun Honey varieties over possible metal/plastic contamination.
5 products
GE HealthCare recalls Revolution Ascend CT over AW Server security vulnerability.
7 products
DonJoy IceMan Classic Cube recalled due to broken connector interrupting cold therapy.
4 products
Dometic is recalling Fan-Tastic Vent Fans (6 part numbers) due to missing hinge pins that may cause lids to detach in transit.

2024 Fly Wing Snake 250 EFI motorcycles recalled for brake pads that may fail in wet conditions.

Shyft is recalling Spartan RV Chassis vehicles because brake lights may stay on, failing to alert other drivers and increasing crash risk.

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.
2 products
Medline is recalling Ancillary Pack-LF and Open Heart Anesthesia ICC-A kits due to potential issues with sterilization and packaging calibration.
58 products
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.
2 products
Good & Gather Sesame Teriyaki Chicken with Rice recalled due to undeclared sesame allergen.

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

Publix Bran Flakes Wheat Cereal recalled over possible plastic contamination.

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.
7 products