State
73,738 recalls have nationwide distribution and so reach Utah. 4,914 additional recalls listed Utah specifically in their distribution scope.
Of the 4,914 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 1,350 (27%) are Severe.
Which agencies issued them
These figures cover only the 4,914 recalls whose distribution notice names Utah specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Arrow International is recalling FlexTip Plus Epidural Catheterization Kits due to potential syringe failures that could cause dural puncture.
Flowonix Medical Inc is recalling Prometra II 20mL implantable infusion pumps due to a firmware defect that may prevent the device from sending error codes or audible alarms for valve system issues.
Terumo is recalling 16 Advanced Perfusion Assembly Pump Guts units because the pump shafts may fail, potentially causing the pump to stop during surgery.
Flowonix Medical Inc is recalling US Clinical 20mL Programmable Pumps because a firmware anomaly may prevent the device from sending error codes or audible alarms during valve system issues.
Flowonix Medical Inc is recalling Prometra II implantable infusion pumps because a firmware anomaly may prevent the device from sending error codes or audible alarms.
Pfizer is recalling 141 bottles of Caduet tablets because defective bottle rims may have allowed moisture to enter, potentially compromising the medication.
Teva Pharmaceuticals USA is recalling 17,436 bottles of Methylphenidate Hydrochloride Extended-Release tablets because the product bottles may be missing desiccant.
Prollenium Medical Technologies is recalling 48,457 kits of Revanesse Versa because the product is labeled with an 18-month expiration date, but it is only approved for 12 months.
Contract Pharmacal is recalling Major Extra Strength Acetaminophen tablets because a foreign prenatal tablet was found in a bottle.
Implant Direct is recalling 78 Legacy 3 dental implants because some packages contain incorrect cover screws and extenders, which may delay surgery or require new procedures.
Pfizer is recalling 128 bottles of Caduet (amlodipine and atorvastatin) because defective bottle rims may have caused inadequate foil sealing, potentially compromising moisture protection.
Lupin Pharmaceuticals is recalling 6,294 bottles of Memantine Hydrochloride Extended Release Capsules because they failed to meet dissolution specifications during stability testing.
C.R. Bard Inc. is recalling 1,300 units of the Bard Intra-abdominal Pressure Monitoring Device due to leaks or disconnects that may cause inaccurate readings.
CooperVision is recalling specific lots of Vertex Toric contact lenses because they were manufactured with an incorrect power.
LivaNova USA Inc is recalling six VNS Therapy SENTIVA Generator Model 1000 units because they were sterilized one additional cycle, failing to meet quality specifications.
Teva Pharmaceuticals is recalling specific bottles of Methylphenidate Hydrochloride Extended-Release tablets because they may be missing the desiccant packet.
GSK is recalling Theraflu Cough Relief packets because the label lacks a warning for people on sodium-restricted diets.
CooperVision is recalling 216 units of Vertex Toric contact lenses because they have an incorrect power than expected.
American Health Packaging is recalling 973 cartons of Raloxifene Hydrochloride 60 mg tablets due to low dissolution results found during stability testing.
Par Pharmaceutical is recalling 9,936 cartons of Frovatriptan Succinate Tablets, 2.5mg, because they are labeled with an incorrect expiration date.
Jayco is recalling 2013-2015 Fifth Wheel Seismic and 2015 Pinnacle trailers because they were built with 6,000lb axles instead of the intended 7,000lb axles.
Bentley is recalling 2018-2020 Bentayga vehicles because side curtain air bags may not inflate properly in a crash, increasing injury risk.
PACCAR is recalling 2020 Kenworth T370 trucks because a missing relay valve may increase brake activation time, lengthening stopping distance and increasing crash risk.
Mercedes-Benz is recalling 2019-2020 G 550 and AMG G63 vehicles because a faulty electrical resistor may deactivate Electronic Stability Program and Anti-lock Brake System.
Kia is recalling 2006-2010 Sedona and 2007-2009 Sorento vehicles because moisture in the ABS module can cause an electrical short and engine compartment fire.