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.
Unruh Fire is recalling one 2018 RAM 5500-based fire truck because its brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.
Forest River is recalling 2018-2019 Cherokee travel trailers because the Federal Placard may list incorrect axle and capacity information, potentially leading to vehicle overload.
Imagine Nation Books is recalling wireless charging pads that can overheat and cause burns or damage to furniture and bedding.
Stainless & Repair is recalling certain 1994-1995 Ford L9000 and 2016-2017 Freightliner M2-112 trucks equipped with Whelen brake lights that may illuminate without the brake pedal being pressed.
Havertys is recalling Beckley Entertainment Hutches because the top shelf can fall, posing an injury hazard. The company has received 12 reports of the shelf falling, including two minor injuries.
BMW is recalling specific 2019-2020 models because knee air bag assemblies may be improperly folded and assembled. This defect could prevent the air bags from deploying as intended, increasing the risk of injury.
GE Healthcare is recalling six NM/CT 860 systems because detector screws may not be secured correctly, potentially compromising mounting redundancy.
GE Healthcare is recalling 37 Discovery NM 830 nuclear imaging systems because detector screws may not be secured correctly, potentially compromising mounting redundancy.
Tom Sturgis Pretzels, Inc. is recalling Little Ones Pretzels because some bags contain a milk allergen not listed on the label.
Viewray is recalling 17 MRIdian Linac Radiation Therapy Systems due to a discrepancy between optimization and planning forward dose calculations.
Siemens is recalling 53 SOMATOM Definition AS CT scanners due to a software issue that may cause scans to abort when using the optional Dual Spiral Dual Energy mode.
GE Healthcare is recalling 35 Optima NM/CT 640 systems because detector screws may not have been secured correctly, potentially compromising mounting redundancy.
Caesar's Pasta, LLC is recalling sweet potato ravioli samples because a sub-ingredient may be contaminated with Listeria monocytogenes or Salmonella.
Advanced Pharma Inc. is voluntarily recalling 560 bags of compounded Hydromorphone 20 mg/100 mL Injectable Solution due to sub-potency. The product was distributed nationwide in the US.
GE Healthcare is recalling 31 NM/CT 850 systems because detector screws may not have been secured correctly, potentially compromising mounting redundancy.
Philips is recalling four Ingenia Ambition MR systems because the Magnet Energization Device may have residual voltage, posing an electrical shock risk to personnel.
GE Healthcare is recalling 11 Discovery NM/CT 670 DR systems because detector screws may not be secured correctly, potentially compromising mounting redundancy.
Igloo is recalling Marine Elite coolers because the stainless-steel latch can automatically lock, posing entrapment and suffocation hazards to children.
GE Healthcare is recalling 57 Discovery NM 630 nuclear imaging systems because detector screws may not be secured correctly, risking loss of mounting redundancy.
Frial SAS is recalling Trader Joe's Saucy Scallops with Mushrooms because the scallop flavor contains low levels of crustaceans not listed on the label.
DePuy Spine is recalling Concorde Lift spinal fusion implants due to a complaint trend of post-operative loss of height and migration.
Fannie May Confections Brands, Inc. is recalling Pixies Caramel and Pecan Clusters because the outer holiday wrap fails to declare pecans, a major allergen.
Iowa Corn Processors is recalling Yellow Corn Flour #600 Unenriched because it may contain pliable blue plastic. The product was distributed to distributors and processors in multiple states and internationally.
Caesar's Pasta, LLC is recalling Beecher's Gluten Free Kale and Rice Gartin because a sub-ingredient may be contaminated with Listeria monocytogenes or Salmonella.
Spagel Brothers, Inc. is recalling Stanganellis Pumpkin Cake Roll because the packaging failed to list soy as an ingredient.