Severity 3 of 5
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
TH Foods Inc is recalling Crunchmaster Multi Grain Baked Gluten-Free Crackers due to possible pieces of glass in the product. The recall affects 7,056 retail units sold in Iowa, Illinois, Indiana, Minnesota, and Wisconsin.
New Dawn Nutrition is recalling Assist and Amend Advanced Digestive Enzyme Formula (Lot #361551, Best By 2022) because it contains undeclared milk, wheat, and soy. Consumers with allergies to these substances are at risk of allergic reaction.
Philips Achieva 3.0T MRI systems may have an incorrectly installed pressure relief valve that could release helium gas and cause injury. Affected units are distributed in the United States and internationally.
DePuy Orthopaedics recalled 7 units of ATTUNE REVISION CEMENTED STEM (16×80mm) because packages labeled as 16×80mm contained 16×130mm stems instead. This size mismatch could cause improper implantation if not caught before surgery.
Hiland Dairy Foods Company LLC is recalling Hiland 100% Pure Apple Juice From Concentrate (4 FL OZ units) due to elevated levels of inorganic arsenic. The recall affects approximately 436,884 units distributed in Arkansas, Missouri, Kansas, Oklahoma, and Texas.
The FDA is recalling AltiVate Anatomic Shoulder Systems due to humeral stem components that may fail to mate properly with broach handles, potentially delaying surgery or requiring revision.
The Terumo Advanced Perfusion System 1 Electronic Patient Gas System is recalled for intermittent initialization failures that disable the primary control interface, requiring use of backup local controls.
Oakworks vascular ultrasound examination tables (models USV1 and USV2) are recalled due to potential weld failure in the tilting mechanism bracket. A failed weld could prevent the table from tilting, affecting patient positioning.
Hitachi Healthcare Americas is recalling ECHELON MRI System table pads because packaging and user manuals lack required disclosure that the pads contain dry natural rubber, a potential allergen. No illnesses have been reported.
PROCEPT BIOROBOTICS is recalling AQUABEAM Handpieces (model HP2000) because the scope tube tip may detach during use, potentially requiring procedural delay or additional intervention to remove the tip from the bladder or prostate.
Ethicon is recalling HARMONICHD 1000i Shears due to a cracked internal component that may cause continuous device activation and result in burns. About 68,960 units have been distributed worldwide.
Polestar is recalling 2021 Polestar 1 vehicles because seat belt retractors may deactivate early, preventing child restraints from securing properly.
Roche Diabetes Care is recalling Accu-Chek Performa test strips because vials may open during shipment, exposing strips to humidity and causing inaccurate glucose readings that could lead to inappropriate diabetes treatment decisions.
Autocar is recalling 2021 Xpeditor and certain 2020-2021 Legend vehicles due to a power steering pump defect that can cause loss of power steering assist and increase crash risk.
Utility Trailer is recalling 2022 VS2RA trailers because incorrect tape on the top foil may cause the sealer plate to separate from the roof, creating a road hazard.
Triple E RV is recalling 550 Unity and Wonder vehicles because a 12-volt wire near the refrigerator exhaust could melt and cause a fire.
Subaru is recalling 2021 Impreza vehicles because the left-front lower control arm weld may fail, causing the arm to separate. This could result in loss of vehicle control and increased crash risk.
Vermeer is recalling 2021 BC900XL, BC1000XL, and BC1200XL brush chippers because the discharge chute may separate and fall off the trailer, creating a road hazard.
Cooper Tire is recalling specific Hercules Roadtour 455 Sport tires due to a manufacturing issue that may cause belt separation, increasing the risk of a crash.
Boise Mobile Equipment is recalling one 2016 Type 3 fire truck because its LED lights may be too bright, potentially affecting other drivers' vision and increasing crash risk.
KZRV is recalling 2018-2022 recreational vehicles with defective Winntec propane regulators that may fail and increase pressure, raising the risk of fire.
Cooper Tire is recalling specific Evolution H/T tires marked with the wrong manufacture date, which could lead to use beyond their recommended service life.
Airstream is recalling certain 2021 recreational vehicles with propane regulator defects that can increase pressure and enlarge flames in gas appliances, creating a fire risk. Dealers will replace the regulator and test the system at no cost.
Escape Trailer is recalling 2019 recreational trailers because window adhesive may fail, causing the vent to detach and increasing crash risk.
Chrysler is recalling 2020 Jeep Wrangler vehicles with 2.0-liter engines because a cracked fuel supply line connector may leak fuel, increasing fire risk.