State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Datascope is recalling 10 custom tubing kits because a seal defect may allow air to enter the housing, causing the balloon to collapse and reducing blood flow in ECMO circuits.
Triangle Pharmanaturals LLC is recalling Raw Form Organics Maeng Da Kratom Ivory White capsules because they may be contaminated with Salmonella.
Vyaire Medical is recalling 3,600 AirLife Infant Resuscitators because the mask may stick to the elbow, making it difficult to disconnect.
Draeger Medical is recalling one Fabius Tiro M anesthesia machine because automatic ventilation may fail if motor position detection is disturbed.
Triangle Pharmanaturals LLC is recalling Lifted Kratom Red Maeng Da products due to potential Salmonella contamination. The recall covers powder and capsule bottles distributed across multiple states.
Triangle Pharmanaturals LLC is recalling Lifted Kratom Gold Bali products because they may be contaminated with Salmonella.
Grato Holdings is recalling Energique herbal supplements because they are marketed as unapproved new drugs based on disease claims.
Triangle Pharmanaturals LLC is recalling Third Eye Kratom White capsules because all Kratom products from the company may be contaminated with Salmonella.
Datascope is recalling 18 custom tubing kits because a seal defect may cause the Better Bladder balloon to collapse, potentially reducing blood flow in ECMO circuits.
Vyaire Medical is recalling 8,124 AirLife Infant Resuscitation devices because the mask may stick to the elbow, making it difficult or impossible to disconnect.
Continental Tire is recalling specific Conti Hybrid HS3 tires because visible cords may cause sudden air loss, increasing the risk of a crash.
Vyaire Medical is recalling 720 pediatric AirLife resuscitation devices because the mask may stick to the elbow, making it difficult to disconnect.
Datascope is recalling two custom pediatric ECMO tubing kits because a seal defect may allow air to enter the device, potentially reducing blood flow.
Datascope is recalling Better Bladder devices in custom tubing kits because seal separation may cause balloon collapse and reduced ECMO blood flow.
Datascope Corporation is recalling 10 units of the BEQ-T 25501 Better Bladder Pack, Custom Tubing Kit. A seal defect may allow air entry, causing balloon collapse and reduced blood flow in ECMO circuits.
Vyaire Medical is recalling 270 pediatric AirLife resuscitation devices because the mask may stick to the elbow, making it difficult or impossible to disconnect.
Vyaire Medical is recalling 42 AirLife Pediatric Resuscitation devices because the mask may stick to the elbow, making it difficult or impossible to disconnect.
Siemens Medical Solutions is recalling Syngo.plaza software due to format errors in study dates and issues with legacy presentation states that could lead to patient misdiagnosis.
Datascope Corporation is recalling BEQ-TOP 22301 Custom Tubing Kits because seal separation may allow air to enter the housing, causing the balloon to collapse and reducing blood flow.
Badger Botanicals LLC is recalling specific Kratom products due to potential Salmonella contamination. The recall covers products manufactured between January 1, 2018, and April 12, 2018.
Vyaire Medical is recalling 24 AirLife Pediatric Resuscitation devices because the mask may stick to the elbow, making it difficult to disconnect.
Datascope is recalling specific custom tubing kits because the Better Bladder device may allow air to enter, potentially reducing blood flow in ECMO circuits.
Datascope is recalling 11 custom tubing kits containing the Better Bladder device due to a seal defect that may cause balloon collapse and reduced blood flow.
Labrada Nutrition is recalling specific lots of Lean Pro 8 Chocolate protein powder due to undeclared egg, a major food allergen.
Zimmer Biomet is recalling 107 Gentle Threads interference screws because overexposure to ethylene oxide sterilization may compromise the sterile barrier, potentially leading to infection.