State
73,737 recalls have nationwide distribution and so reach Missouri. 8,500 additional recalls listed Missouri specifically in their distribution scope.
Of the 8,500 recalls naming Missouri we have scored against our rubric, 1,339 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,203 (26%) are Severe.
Which agencies issued them
These figures cover only the 8,500 recalls whose distribution notice names Missouri specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Sanofi-Aventis is recalling 7,451 vials of Elitek (rasburicase) because routine stability testing showed enzyme activity levels were out of specification.
Calvin Scott & Co. is recalling Thyroid 1 Gr tablets because light-sensitive products were repackaged in transparent pouches, violating CGMP standards.
Calvin Scott & Co. is recalling specific lots of Phendimetrazine capsules because light-sensitive products were repackaged in transparent pouches, violating CGMP standards.
Calvin Scott & Company is recalling specific lots of Phentermine HCL 37.5 mg tablets because they were repackaged in transparent pouches, violating light-sensitivity requirements.
Calvin Scott & Company is recalling Phentermine HCL 30mg capsules because light-sensitive products were repackaged in transparent pouches, violating CGMP standards.
Calvin Scott & Company is recalling Phentermine 15mg capsules because light-sensitive products were repackaged in transparent pouches, violating CGMP standards.
Calvin Scott & Company is recalling specific lots of Phendimetrazine 35mg tablets because light-sensitive products were repackaged in transparent pouches.
Calvin Scott & Company is recalling Thyroid Neutral Tabs 2 gr because light-sensitive tablets were repackaged in transparent pouches, violating CGMP standards.
Smith & Nephew is recalling 528 units of the Polarstem Collar Reamer Guide due to a product design issue. The devices were distributed worldwide and in the US.
Calvin Scott & Company is recalling specific lots of Phentermine HCL tablets because light-sensitive products were repackaged in transparent pouches.
Calvin Scott & Company is recalling specific lots of Phendimetrazine 35mg tablets because they were repackaged in transparent pouches, violating CGMP requirements for light-sensitive drugs.
Calvin Scott & Company is recalling Phentermine HCL 30mg capsules because they were repackaged in transparent pouches, exposing the light-sensitive medication to potential degradation.
Calvin Scott & Company is recalling specific lots of Phentermine HCL tablets because they were repackaged in transparent pouches, violating CGMP requirements for light-sensitive drugs.
Calvin Scott & Co. is recalling Hydrochlorothiazide 25mg tablets because light-sensitive products were repackaged in transparent pouches.
Shanghai United Imaging Healthcare Co., Ltd. is recalling three uMI 550 PET/CT systems because a software defect may prevent the CT Hounsfield unit curve from displaying in real time during specific scans.
Calvin Scott & Company is recalling Hydrochlorothiazide 50mg tablets because light-sensitive products were repackaged in transparent pouches, violating CGMP standards.
CareFusion 303, Inc. is recalling Alaris Pump Module Model 8100 units because LED display segments may appear dim, potentially affecting the visibility of infusion or patient monitoring values.
Altec is recalling 2018-2020 EC505 and EC655 vehicles because grapple tines may loosen, risking loss of load control.
Altec is recalling 2015-2018 aerial devices because a software issue can cause the boom to move unexpectedly during an engine cycle, increasing injury risk.
Volvo is recalling 2018-2020 XC60 vehicles because front wiper nuts may be loose, potentially impairing visibility and increasing crash risk.
Equipment Technology is recalling 2020 ETI ETC 37 IH aerial lift trucks because improper welds and steel thickness may cause the platform to fall unexpectedly.
Oshkosh is recalling 172 2020 S-Series vehicles because a pressure switch defect may cause air leaks, increased braking distance, or brake light failure.
Oberto Snacks is recalling 309 pounds of smoked sausage due to misbranding and an undeclared soy allergen. No adverse reactions have been reported.
Autocar is recalling 78 model year 2019 Xpeditor vehicles up-fitted with an aftermarket power take off (PTO) because they may stall or hesitate, increasing the risk of a crash.
woom bikes USA is recalling about 1,900 children's helmets because they do not meet federal safety standards, posing a risk of head injury.