State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Maquet Cardiovascular is voluntarily recalling 72,000 custom tubing packs for oxygenators due to a potential risk of endotoxin exposure.
C.R. Bard is recalling 21,412 ArcticGel Pads used with the Arctic Sun Temperature Management System because of complaints regarding restricted or inaccurate flow rates.
ICU Medical is recalling 49 units of the Diana Automated Compounding System because it may not meet accuracy specifications when mixing volumes under 5ml.
Morrison Milling is recalling HEB Original Seasonal Fish Fry Mix because it may contain small metal fragments from a wire mesh sifter.
Synthes (USA) Products LLC is recalling 317 units of SYNTHECEL Dura Repair because the device may adhere to anatomical structures, posing risks if removal is attempted.
YTL International is recalling about 17,000 drywall lifts because they can fail and drop loads, posing an injury risk. No injuries have been reported.
Arjo is recalling 1,596 Concerto Basic Shower Trolleys because bolts connecting the stretcher to the hydraulic piston and tilting mechanism may become loose.
The Clorox Company is recalling Hidden Valley Original Ranch dressing because some bottles are missing the soy lecithin ingredient declaration.
Philips is recalling EPIQ diagnostic ultrasound systems because fasteners securing the control panel may loosen, potentially causing the assembly to detach.
Maquet Cardiovascular is voluntarily recalling Rotaflow Centrifugal Pump custom tubing packs due to a potential risk of endotoxin exposure.
Intuitive Surgical is recalling da Vinci S Surgical System user manuals because using certain instruments with ablation probes can increase microscopic metallic particulates.
Morrison Milling is recalling Marie Callender's Low Fat Southwestern Corn Bread Mix because it may contain small metal fragments from a wire mesh sifter.
Philips Medical Systems is recalling 82 Ingenuity CT systems due to a software error that may prevent the automatic transmission of image data to remote devices.
ICU Medical is recalling 57 Diana Automated Compounding Systems because they may not accurately mix volumes under 5ml.
Morrison Milling is recalling Pioneer Original Buttermilk Pancake & Waffle Mix because it may contain small metal fragments from a wire mesh sifter.
Cosmetic Labs LP is recalling L'Bri Pure N' Natural Nutri Aloe Health Juice Drink because it contains sodium metabisulfite, an ingredient not listed on the label.
Morrison Milling is recalling Conestoga Buttermilk Pancake Mix because it may contain small metal fragments from a wire mesh sifter.
Morrison Milling is recalling American Blue Ribbon Multigrain Pancake Mix because it may contain small metal fragments from a wire mesh sifter.
Stryker is recalling 286 SurgiCounter scanners because they may display error messages and fail to display software version numbers correctly in the SC360 application.
Morrison Milling is recalling Hartz Krispy Chicken 'N' Rolls Milk Dip because it may contain small metal fragments from a wire mesh sifter.
Morrison's Country Style Corn Bread Mix is being recalled because it may contain small metal fragments from a wire mesh sifter.
Morrison Milling is recalling Fletcher's Corny Dog Mix because it may contain small metal fragments from a wire mesh sifter.
Morrison Milling is recalling Champs Chicken Batter Mix because it may contain small metal fragments from a wire mesh sifter.
Morrison Milling is recalling On The Border Tempura Batter because it may contain small metal fragments from a wire mesh sifter.
C.R. Bard is recalling 1.4 million Bardex Foley catheters because the instructions for use list an incorrect inflation volume.