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

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
Finesaler recalls Alain Milliat Orange Marmalade 300g jars over possible glass contamination.

DonJoy IceMan Classic Cube recalled due to broken connector interrupting cold therapy.
4 products
On-X is recalling Model ONXMC-25/33 Mitral Heart Valve due to incomplete testing before distribution.

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.

The Brownie Baker is recalling Cafe Nouria Blueberry Muffin due to undeclared walnuts, which pose a risk to those with nut allergies.

Youth sweatshirts with drawstrings are recalled due to a strangulation hazard, as they violate federal safety regulations for children's wear.

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.

EVLWZL and Gunugu mattresses are recalled for violating federal flammability standards, posing a serious fire and injury risk.

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.
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