State
73,219 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 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Newly Weds Foods is recalling approximately 6.5 million pounds of breader product due to potential Salmonella contamination. The affected product was distributed across the United States and Canada.
Newly Weds Foods is recalling patty seasoning due to potential Salmonella contamination. The affected product was distributed across the US and Canada.
Newly Weds Foods is recalling A99744 Breader product due to potential Salmonella contamination. The product was distributed across the United States and Canada.
Newly Weds Foods is recalling approximately 6.5 million pounds of B94464 breader product due to potential Salmonella contamination. Consumers should not use this product.
Newly Weds Foods is recalling A97176 BREADER X3 breader products that may contain Salmonella. The recall affects products with specific lot codes distributed across multiple U.S. states and Canada.
Newly Weds Foods is recalling Kuro Buta Sausage Seasoning distributed across 27 US states and Canada due to potential Salmonella contamination.
Newly Weds Foods recalls wiener and bologna products due to potential Salmonella contamination. Products were distributed across multiple U.S. states and Canada.
Newly Weds Foods is recalling Cajun Sausage Seasoning (code YE675289) because it may contain Salmonella. The product was distributed to 27 states and Canada.
Newly Weds Foods is recalling Inject for Cajun Turkey products due to potential Salmonella contamination. The product was distributed across 27 U.S. states and Canada.
Drive board malfunction in TrackMaster TMX428 treadmills can cause unexpected belt reversal or acceleration, creating fall and impact injury risks. 376 units affected.
TEI Biosciences recalled 7,264 units of PriMatrix Ag Fenestrated dermal repair scaffolds nationwide due to possible out-of-specification endotoxin test results caused by testing methodology defects.
Intuitive Surgical is recalling 46,033 da Vinci Xi/X Tip-Up Fenestrated Graspers worldwide due to a manufacturing issue that can cause grip breakage, potentially allowing stainless steel fragments to enter the patient.
TEI Biosciences is recalling 4,159 units of PriMatrix Dermal Repair Scaffold nationwide due to possible out-of-specification endotoxin test results. Quality control issues during testing led to this recall.
TEI Biosciences is recalling 22,163 units of SurgiMend PRS collagen matrices due to endotoxin testing deficiencies that may have resulted in contaminated products being distributed. No injuries have been reported.
T.A.G. Medical Products is recalling BETTA LINK SR Reusable Fishmouth Guides (Part Number 110045151) because the drill guides may bend during surgical use and result in metal shavings. The risk to patients includes potential injury.
Waldemar Link GmbH & Co. KG recalled LinkSymphoKnee Distal Femoral Augments due to incorrect screw orientation during manufacturing. The fixation screw may be inserted through the wrong side of the augment, affecting 20 units distributed across seven US states.
Full Vision Inc is recalling 1,416 TrackMaster GE T2100-ST2 220V treadmills worldwide due to a drive circuit board defect that can cause the treadmill to stop suddenly, reverse unexpectedly, or accelerate forward, posing a risk of falls or injury.
Cargill is recalling Trisodium Citrate Dihydrate due to potential metal contamination. The food additive ingredient was distributed to manufacturers and operations in multiple states and Canada.
Polestar is recalling certain 2023 Polestar 2 vehicles due to a defect in the front left lower ball joint that could cause loss of steering control. Owners should contact their dealer for a free inspection and replacement.
TEI Biosciences is recalling 9,215 units of SurgiMend PRS Meshed, a surgical collagen matrix, due to possible out-of-specification endotoxin test results.
The FDA has recalled BETTA LINK SR Knotless Implant Kits because the drill guides may bend during surgical procedures, potentially releasing metal shavings. This affects surgeons and patients undergoing orthopedic ligament and tendon repair procedures worldwide.
TEI Biosciences recalled approximately 3,992 units of SurgiMend MP surgical implants nationwide due to issues with endotoxin testing procedures that may have resulted in unreliable test results.
BMW is recalling 2023 740i, 760i, and i7 vehicles because the dashboard Interaction Bar may fail to activate defrosting or hazard lights.
DeRoyal Industries is recalling 40 units of STURDI STRAINER TRAY STANDARD procedure packs nationwide due to potentially compromised outer package seals that could affect sterility.
DeRoyal Industries is recalling 3 packs of Pelvic Exam Trays because the outer package seals may be open or compromised, potentially affecting the sterility of the medical procedure packs.