State
73,106 recalls have nationwide distribution and so reach Missouri. 8,493 additional recalls listed Missouri specifically in their distribution scope.
Of the 8,493 recalls naming Missouri we have scored against our rubric, 1,344 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,882 (22%) are Severe.
Which agencies issued them
These figures cover only the 8,493 recalls whose distribution notice names Missouri specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Daimler Coaches is recalling 2011-2016 Setra coaches because wheelchair lift warning beacons may be too dim, increasing injury risk.
Randder 2-Pack Liquid Fuel Bottles in 750mL and 1500mL sizes sold on Amazon are recalled because their closures do not meet child-resistant requirements under the Children's Gasoline Burn Prevention Act, posing a risk of burns and poisoning to children.
Alipotec Raiz de Tejocote dietary supplements are being recalled because they contain toxic yellow oleander instead of tejocote. All 280 bottles were distributed nationwide.
Eugia US LLC is recalling Methocarbamol Injection nationwide due to particulate matter contamination. The FDA classified this as a Class I recall affecting lot 3MC23011 (expiration 11/30/2026).
Spencer is recalling 2024 Pumper vehicles because a firmware defect in specific electrical nodes may cause overloaded circuits and increase the risk of fire.
Tesla is recalling certain 2024 Cybertruck vehicles because the accelerator pedal pad may dislodge and become trapped by the interior trim, potentially causing unintended acceleration and crash risk.
Certain patient lift models may have a hanger bar that could come loose during use, potentially causing patient falls. Approximately 10 units distributed to TX, IL, OK, and CA are affected.
Microbiologics Inc recalls KWIK-STIK quality control kits contaminated with Aspergillus brasiliensis fungus. Users may observe unexpected fungal growth when using affected control material.
Medline is recalling certain lots of adult portable bed rails that were manufactured after the mandatory compliance date but failed to meet required safety standards, potentially posing a fall risk.
Philips CT scanner software upgrade may cause the patient tabletop to move unexpectedly during scan initialization, posing collision risk to nearby operators or bystanders.
Whitley Peanut Factory is recalling Deluxe Nut Mix due to undeclared allergens (peanuts, milk, soy, wheat, and sesame) not listed on the product label. Consumers with allergies should not consume this product.
ConvaTec is recalling 63 market units of CarboFlex odor control dressings that fail to meet sterility assurance requirements. Affected lots were distributed in six states.
Synovo Production is recalling 764 acetabular fixation cups marketed without FDA clearance or approval. These hip replacement components were distributed nationwide in Washington state.
Boston Scientific's EndoVive 20Fr PEG kit may have a blocked connector preventing proper guidewire advancement during placement, potentially requiring emergency intervention.
Lupin Pharmaceuticals recalls Rifampin Capsules USP 300mg nationwide due to subpotency—the drug contains less active ingredient than labeled. Affected lot: A201064, expiring March 2024. 26,352 bottles involved.
Toyota is recalling 2023–2024 Prius and Prius Prime vehicles because water may enter the rear door switch, causing it to short circuit and allow the rear door to open unexpectedly while driving or during a crash.
Synovo Production recalled 496 femoral resurfacing cup components that were marketed without FDA clearance. These hip implant components were distributed in the United States.
Boston Scientific is recalling EndoVive 20 Fr feeding tubes due to potential blockage during placement that may prevent guidewire advancement. This could lead to procedure complications including bleeding, gastric leakage, or aspiration.
Medline is recalling 79 Bed Assist Bars that failed to comply with federal safety standards for adult portable bed rails. The products were manufactured after the compliance deadline.
Teva Pharmaceuticals recalls Isotretinoin 40mg capsules for exceeding specification limits in potency. No illnesses reported.
Qiagen Sciences is recalling 168 units of the EZ2 Connect MDx-IVD nucleic acid isolation device due to insufficient welding that causes heater cable embrittlement and device malfunction, resulting in sample loss during testing.
Forest River and Dynamax are recalling multiple 2018–2024 travel trailer models due to LED backlight circuit boards in cooktop ranges that may overheat and create a fire risk. Dealers will disconnect and remove the LED backlight wiring at no charge.
Boston Scientific's EndoVive 20Fr PEG Kit may have a blocked connector that prevents the guidewire from advancing during placement, potentially causing complications including bleeding and aspiration.
RayStation radiation therapy planning software versions 8B through 2024A contain a use error that can incorrectly select silicon material for silicone gel polymer implant dose calculations, potentially resulting in incorrect radiation doses.
Synovo Production is recalling 1,681 acetabular bearing components that were marketed without FDA clearance.