State
73,824 recalls have nationwide distribution and so reach Missouri. 8,501 additional recalls listed Missouri specifically in their distribution scope.
Of the 8,501 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 2,204 (26%) are Severe.
Which agencies issued them
These figures cover only the 8,501 recalls whose distribution notice names Missouri 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 strengths and dosage forms of Heparin sodium because the product may contain synthetic or natural latex without proper labeling.
Advanced Pharma Inc. is recalling Sodium Phosphate products because they may contain latex but lack proper labeling. The recall covers all strengths and dosage forms distributed nationwide.
BioMerieux SA is recalling Ceftriaxone ETEST kits due to a potential performance issue affecting strain categorization.
Advanced Pharma Inc. is recalling Calcium Gluconate products because they may contain latex without proper labeling.
Advanced Pharma Inc. is recalling all strengths and dosage forms of Sodium Citrate because the product may contain latex without proper labeling.
Siemens Medical Solutions is recalling 4,095 AXIOM Sensis diagnostic computers because dust accumulation can cause system failures, potentially interrupting clinical treatments.
Advanced Pharma Inc. is recalling all strengths and dosage forms of Potassium Phosphate because the product may contain latex but lacks proper labeling.
Advanced Pharma Inc. is recalling Cardioplegic Solution Maintenance due to a labeling error regarding potential latex content.
Advanced Pharma Inc. is recalling all lots of Midazolam HCl because the product may contain synthetic or natural latex.
Advanced Pharma Inc. is recalling all lots of Ketamine HCl because the product may contain synthetic or natural latex.
Advanced Pharma Inc. is recalling all lots of Succinylcholine Chloride because the product may contain latex but lacks proper labeling.
Advanced Pharma Inc. is recalling all lots of Ephedrine Sulfate because the product may contain latex but lacks proper labeling.
Advanced Pharma Inc. is recalling all lots of Morphine Sulfate because the product labeling does not indicate that it may contain synthetic or natural latex.
Advanced Pharma Inc. is recalling all strengths and forms of Rocuronium Bromide because the product may contain latex without proper labeling.
Advanced Pharma Inc. is recalling all lots of Adenosine because the product may contain latex but lacks appropriate labeling.
Mylan Pharmaceuticals is recalling Tarina Fe 1/20 tablets due to chemical contamination from paint thinner vapors during manufacturing.
Bard Access Systems is recalling 4,500 units of StatLock IV Premium Catheter Stabilization Devices because they may contain incorrectly sized retainer clips.
Beckman Coulter is recalling Microalbumin Reagent Lot M609458 because it may recover outside the lower limit of the published insert range for Urine Protein Control Level 1.
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.