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.
Decked is recalling CargoGlide Drawer System Brackets because oversized holes may cause the unit to detach from the tailgate, increasing injury risk.
CFMOTO is recalling certain 2022-2023 700CL-X motorcycles because ABS software may delay braking when the hand brake lever is squeezed multiple times, increasing crash risk. Dealers will update the software free of charge.
XOS is recalling 2021-2022 SV05 vehicles because the electronic parking brake may fail to engage, increasing the risk of a crash.
Forest River is recalling 2024 Coachmen and Forest River travel trailers because reversed electrical plug blades may cause outlet failure and increase fire risk.
Forest River is recalling 2022-2024 Forester and Sunseeker motorhomes because the park brake signal wire may not be connected to the battery control center, allowing the slideroom to unexpectedly extend during transit and increase crash risk.
Airstream is recalling certain 2019-2024 motorhomes because their tire labels show incorrect pressure and size information. This can lead to under-inflated or incorrectly sized tires, increasing the risk of crashes.
USDA FSIS issued a public health alert for Pruski's Market jerky products due to undeclared soy. Consumers are urged not to consume the affected items.
Tractor Supply is recalling about 7,500 Red Shed® Hammock Swing Chairs because the plastic buckle supporting the back can break while someone is seated, causing a fall. The company has received 13 reports of buckle or stitching failures, including three falls.
Jayco is recalling 2023-2024 motorhomes where corrosion in an electrical connector can disable the instrument panel, preventing display of the speedometer and warning lights.
LAOION children's cups sold on Amazon contain lead in solder on the cup bottom and have lids that can crack, creating choking and laceration risks. About 200 units were sold from March to May 2023.
BMW is recalling certain 2024 BMW X3 and related models due to steering gear that may not have been properly tightened, which can loosen and cause loss of vehicle control. Dealers will replace the steering gear free of charge.
Target is recalling about 1,850 units of its 13-Piece Toy Mushroom Peg Sorters because the mushroom stems can detach, posing a choking hazard to young children. No injuries have been reported.
Philips EasyDiagnost Eleva DRF digital radiographic systems mounted on ceilings may fail and fall. 40 units nationwide are being recalled due to potential ceiling mount failure.
Gills Onions, LLC is recalling Cross Valley Farms slivered yellow onions due to potential Salmonella Thompson contamination. The recall affects 6,400 pounds distributed across the United States and Canada.
Stryker Corporation is recalling 2,321 units of Disposable Spetzler-Malis Bipolar Forceps because the product label incorrectly shows a 54-month shelf life when the actual shelf life is 36 months.
B. Braun Medical is recalling 175,000 units of bulk largebore male LL fittings due to a manufacturing defect that may cause leakage, potentially increasing bloodstream infection risk.
St. Jude Medical is recalling CardioMEMS Patient Electronic System (Model CM1100) because the power connector plug may become damaged and frayed if bent beyond 90 degrees. This could cause device malfunction or electrical hazard.
B. Braun is recalling FT1000S Fluid Transfer Sets due to a manufacturing defect that may cause leakage. This could delay therapy, increase infection risk, and expose healthcare workers to hazardous medication.
Stryker Corporation recalls 2,321 units of Disposable Spetzler-Malis Bipolar forceps due to incorrect expiration dates on product labels. The actual shelf life is 36 months, but labels indicate 54 months.
The Cookie Factory LLC is recalling Stewarts Chocolate Chip Cookies (6 oz packages) because they contain undeclared macadamia nuts, posing an allergen risk to consumers with macadamia nut allergies.
Philips has recalled certain surgical C-arm imaging systems delivered to Puerto Rico because they lack required warning labels and are missing a critical Source-to-Skin Distance Spacer component.
Family Dollar Stores is recalling 329,044 CLEARBLUE pregnancy test kits that were stored outside labeled temperature requirements from June to October 2023 at stores in 22 states.
B. Braun Medical is recalling Allergan Universal Fill Kits for tissue expanders due to a manufacturing defect that may cause device leakage. Leakage can delay treatment, increase infection risk, and potentially create life-threatening situations.
Cookies-n-Milk Incorporated is recalling Edible Cookie Dough Chocolate Chip due to undeclared peanut butter. The product contains peanut butter dough mislabeled as chocolate chip, posing a risk to consumers with peanut allergies.
Carestream Health is recalling 2,402 DRX-Revolution Mobile X-Ray Systems due to potential electrical failure in the generator causing thermal overload. The system becomes inoperable and may produce loud noise, burnt smell, and smoke.