Severity 4 of 5
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.
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.
Spartan Motors is recalling 66 model year 2015 K3 chassis because tag axle suspension hangers may move, causing the axle to shift off center and increasing crash risk.
Grand Design is recalling specific 2015-2016 Reflection and Solitude trailers because wheel studs may break, potentially causing the wheel to detach and increasing crash risk.
Baxter Healthcare is recalling 196,128 containers of 0.9% Sodium Chloride Injection due to lack of sterility assurance and leak complaints.
Baxter Healthcare is recalling 7,444 containers of Clinimix E 5/20 due to a lack of assurance of sterility and increased leak complaints.
Spice N' More Corp. is recalling various brands of cumin powder because the product may contain undeclared peanut protein.
Pega Medical Inc. is recalling 7 units of the 4.8mm GAP Nail because of failures at the distal cortical screw holes, primarily in patients with specific bone conditions.
Starwest Botanicals is recalling Blue Cheese Jalapeno Steak due to the presence of peanut protein. The product was distributed to one customer in Missouri.
Medtronic is recalling 6,040 Model 5392 temporary pacemakers because specific AA batteries may fail to connect, potentially stopping pacing therapy.
Starwest Botanicals is recalling 45-pound bags of BAM124 Chili Powder Salt Free because it contains peanut protein. The product was distributed to one customer in Missouri.
Maternal Science Inc. is recalling Healthy Mama Boost It Up Mighty Mango Protein Drink because it contains undeclared milk.
AL'S PICADERA is recalling Tres Leches Cake because the label fails to declare soy as an ingredient. The product was distributed in Puerto Rico.
The Spicemill LLC is recalling 99 bottles of Ground Cumin in Connecticut due to undeclared peanut protein.
Fiesta Pacific is recalling Brown Label Horchata Post Mix Fountain Syrup because a formulation error and lack of preventive processes allow potentially harmful bacteria, including Clostridium botulinum, to grow.
Zenobia Company LLC is recalling My Spice Sage Ground Cumin because it may contain undeclared peanut protein. The recall covers 1,467 units sold nationwide.
Starwest Botanicals is recalling 180 lbs of Sweet Curry Powder because it contains peanut protein. The product was distributed to one customer in Missouri.
Maternal Science Inc. is recalling Healthy Mama Boost It Up Mango with Ginger Protein Drink because it contains undeclared milk.
KTM is recalling 409 model year 2015 690 Enduro R motorcycles because the rear brake line may be damaged, potentially causing a loss of braking ability and increasing crash risk.
Starwest Botanicals is recalling 20 lb. bags of Caribbean Jerk Seasoning due to the presence of peanut protein.
American Spice & Seasoning, Inc. is recalling Adkins Barbecue Spice because it contains cumin from a recalled supplier.
BD Biosciences is recalling 72 BD FACSCalibur instruments because some have circuit breakers with incorrect amperage ratings, which may fail to open during over-current situations.
Brinkhoff & Monoson Inc is recalling Archer Farms ground cumin because it may contain undeclared peanut allergens.
Prima Spice, Inc. is recalling Chef's Delight Ground Cumin 5.0 lb jugs due to possible peanut protein contamination.
Brinkhoff & Monoson is recalling Dark Chili Powder distributed by The Fresh Market because it contains cumin that may be contaminated with undeclared peanut allergens.
Gilster-Mary Lee Corp. is recalling Honey & Oat Mixers dry cereal because it contains undeclared almonds, a major food allergen.
DePuy Orthopaedics is recalling 54 units of the RECLAIM Assembled Implant Inserter Adaptor because the instrument may fracture during surgery, potentially leaving plastic pieces in the patient.