State
73,824 recalls have nationwide distribution and so reach Utah. 4,916 additional recalls listed Utah specifically in their distribution scope.
Of the 4,916 recalls naming Utah we have scored against our rubric, 524 (11%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,351 (27%) are Severe.
Which agencies issued them
These figures cover only the 4,916 recalls whose distribution notice names Utah specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Advanced Pharma Inc. is recalling all lots of Atropine Sulfate because the product may contain latex but lacks appropriate labeling.
Advanced Pharma Inc. is recalling all Esmolol HCl products because the labeling does not indicate that the products may contain synthetic or natural latex.
RB Manufacturing is recalling Schiff Move Free Advanced Plus MSM & Vitamin D3 tablets due to incorrect packaging.
Sun Pharmaceutical Industries is recalling 13,200 bottles of Children's Cetirizine Hydrochloride Chewable Tablets due to out-of-specification tablet hardness.
Medtest Holdings is recalling Pointe Scientific Chemistry Controls Level I and II because the original mean assigned to the controls was too high, resulting in a new assigned mean outside the published range.
Strides Pharma Inc. is recalling Benzonatate capsules due to out-of-specification preservative levels. The FDA classified this as a Class III recall.
Qualitest Pharmaceuticals is recalling 109,620 bottles of Hydrocortisone Lotion, USP, 2.5% because the product is superpotent, meaning it contains more active ingredient than specified.
Volkswagen is recalling 2017 Jetta vehicles because the VIN on the body does not match the VIN plate near the windshield, violating federal certification regulations.
Pierce Manufacturing is recalling 1999-2013 fire trucks with electric All-steer rear steering due to improperly heat-treated axle shafts that may break.
KZRV is recalling 2016-2018 Venom fifth-wheel travel trailers with outside kitchens because a missing copper pipe may cause the gas line to melt and start a fire.
Jayco is recalling 2018 Eagle TT 330RSTS trailers because the Federal Placard lists an incorrect Gross Axle Weight Rating, which could lead to overloading and loss of control.
VanLeigh is recalling 2015-2018 Vilano fifth-wheel recreational trailers because the spare tire winch may not be properly fastened, posing a crash risk if the tire falls off.
Gulf Stream is recalling 2015-2018 Vista and Vintage Cruiser travel trailers because the tire label lists incorrect tire specifications, which could lead to installing the wrong replacement tires.
CPSC is recalling about 28,000 Kobalt and Greenworks cordless electric lawn mowers because the circuit board can short circuit and catch fire. No injuries have been reported.
Gulf Stream is recalling 2018 Cruiser VN23BHS travel trailers because the Federal Certification Label overstates axle capacity by 700 lbs, posing a crash risk.
Forest River is recalling 2016-2017 Vibe recreational trailers because the Federal Placard lists incorrect tire size and pressure information, which could lead to improper tire maintenance.
Vantage Mobility is recalling 2017 Chrysler Pacifica vans modified for wheelchair accessibility because crossed rear brake lines may render the anti-lock brake system ineffective.
Eldorado Mobility is recalling 2017 Amerivan 10 lowered-floor vehicles because trailing arm mounts may break, potentially causing loss of steering control.
Jaguar is recalling 2018 F-TYPE vehicles with Highline headlamps because the turn signal reminder may not flash or chime faster if a signal fails, increasing crash risk.
Extech is recalling specific digital clamp meters because they may display incorrect voltage readings, posing an electrocution risk to operators.
Key Pharmacy and Compounding Center is recalling TRI MIX 40/30/4 injection vials because the firm cannot assure the sterility of the product.
Key Pharmacy and Compounding Center is recalling 17 vials of TRI MIX 20/30/2 injection due to a lack of assurance of sterility.
Key Pharmacy and Compounding Center is recalling specific lots of Folinic Acid MDV Injection due to a lack of assurance of sterility.
Key Pharmacy and Compounding Center is recalling specific lots of Testosterone Cypionate injections because the firm cannot guarantee the products are sterile.
Key Pharmacy and Compounding Center is recalling specific lots of Papaverine/Phentolamine injection because the firm cannot assure the sterility of the product.