State
72,969 recalls have nationwide distribution and so reach Missouri. 8,465 additional recalls listed Missouri specifically in their distribution scope.
Of the 8,465 recalls naming Missouri we have scored against our rubric, 1,334 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,870 (22%) are Severe.
Which agencies issued them
These figures cover only the 8,465 recalls whose distribution notice names Missouri specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Bendix is recalling specific Knorr-Bresme brake chambers for buses due to improper manufacturing that can cause air leaks and increase fire risk.
KidKraft Farm to Table play kitchens are being recalled because clothing can catch on the accessory hooks. A 23-month-old child died from strangulation and asphyxia in February 2023.
The Cosco 2-Step Kitchen Stepper is being recalled because the safety bar can detach or break while in use. Thirty-four reports include two incidents resulting in head injuries.
IKEA 365+ VÄRDEFULL garlic presses are being recalled because small metal pieces can detach, posing laceration and ingestion hazards. Three lacerations have been reported globally.
Baby Loren Morning children's cotton loungewear dresses are being recalled because they violate the flammability standards for children's sleepwear. About 340 units are affected.
Tegu Magnetic Floating Stackers are being recalled because magnets can loosen and detach, violating the mandatory standard for toy magnets. Thirty-one reports of magnets separating have been received.
RIDGID 18Volt Brushless 21-Degree and 30-Degree Framing Nailers are being recalled because the dual action engagement system can malfunction and involuntarily discharge a nail. About 64,000 units affected.
Premier Trailer Solutions is recalling 2024 Reel and Pole trailers because improperly installed oil seals may leak oil onto the brake system, reducing braking ability.
Amazon Basics Premium Foam Eurotop Mattresses are being recalled because they violate a mandatory flammability standard for mattresses. About 2,700 units are affected.
Leatherman Charge Plus and Charge Plus TTi multi-tools are being recalled because the tip of the knife blade does not fully fold into the handle, posing a laceration hazard. About 17,000 units affected.
Storyteller Overland is recalling 2023 Mode LT recreational vehicles because improperly tightened shore power inlets may overheat and cause a fire. Dealers will replace the inlets free of charge.
The Covidien Nellcor Bedside SpO2 Patient Monitoring System is being recalled because alarms may not be heard or recognized, which the manufacturer links to treatment delay. 264,790 units are affected.
HSG Procedure Trays are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 171 units are affected.
GE HealthCare Discovery MR750w 3.0T MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.
Biofinity Toric Multifocal Contact Lenses are being recalled because lens blisters may have an incomplete or leaking seal, which may render them unsterile. 827 units are affected.
USDA FSIS issued a public health alert for frozen tortellini that may contain undeclared soy and sesame. Consumers with allergies should not consume the product.
The Medtronic CareLink SmartSync Patient Connector is being updated because in prior application versions the abort window during an induction test limited the user's ability to cancel high voltage therapy. 22,091 devices affected.
GE HealthCare SIGNA Architect AIR MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.
Epinephrine Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL vials compounded by Imprimis NJOF are being recalled because of subpotent assay results during stability testing. 6,880 vials affected.
Endosee System Convenience Kits with IV Tube are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 475 units affected.
Ritz Cracker Sandwiches 20 count variety packs are being recalled because of undeclared peanut allergens due to mispackaging. 13,872 cases are affected.
Endosee System Convenience Kits are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 991 units are affected.
The Azurion 7 M20 fluoroscopic x-ray system is being recalled because of the potential for bolts connecting the gearbox to the mounting flange of the C-arm to become loose. 78 units affected.
Budesonide Inhalation Suspension 0.5 mg/2 mL is being recalled for lack of assurance of sterility after a market complaint was received for leakage and an empty ampoule. 13,680 ampoules affected.
The Natus Brain Monitor Breakout Box is being recalled after two complaints that the left side labeling showed impedance for the right side. 27 units are affected.