State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Cardiovascular Systems Inc. is recalling 1,396 Saline Infusion Pumps that may switch to stand-by during use, requiring a reset to continue treatment.
Cardinal Health 200, LLC is recalling Jackson-Pratt Silicone Flat Drains because the product seal may be compromised, potentially compromising sterility and increasing the risk of infection.
Datascope is voluntarily removing 996 units of SENSATION PLUS Intra-Aortic Balloon Catheters due to internal pressure testing failures related to tip seal leaks.
Cardinal Health 200, LLC is recalling Jackson-Pratt Silicone Round Drains because the product seal may be compromised, potentially compromising sterility and increasing infection risk.
Beckman Coulter is recalling UniCel DxH 800 systems because a software issue may cause erroneous white blood cell differential results.
Beckman Coulter is recalling UniCel DxH 600 systems due to a software issue that may cause erroneous white blood cell differential results.
Rich Products Corp is recalling 7 oz pizza dough balls because the flour used may be contaminated with E. coli 0121.
Cardinal Health 200, LLC is recalling specific lots of Jackson-Pratt Silicone Round Drains because the product seal may be compromised, potentially increasing the risk of infection.
Medtronic is recalling specific MRI-conditional CRT-D devices due to an unexpected transient mode switch behavior detected during systems testing.
Cardinal Health 200, LLC is recalling Jackson-Pratt Hemaduct Silicone Round Drains because the product seal may be compromised, potentially compromising sterility and increasing infection risk.
Rich Products Corp is recalling Artisan Crust Pizza Dough because the flour used may be contaminated with E. coli O121.
Cardinal Health is recalling specific lots of Jackson-Pratt Hemaduct Cardiothoracic Silicone Round Drains because the product seal may be compromised, potentially compromising sterility and increasing infection risk.
Terex Advance is recalling 2017 Front Discharge Concrete Mixers because welds on the 250-gallon water tank filler neck may fail, posing an injury risk.
Cardinal Health 200, LLC is recalling Jackson-Pratt Silicone Round Drains because the product seal may be compromised, potentially compromising sterility and increasing infection risk.
Cardinal Health 200, LLC is recalling Jackson-Pratt Hemaduct Silicone Flat Drains because the product seal may be compromised, potentially compromising sterility and increasing infection risk.
Cardinal Health is recalling specific lots of Jackson-Pratt Silicone Flat Drains because the product seal may be compromised, potentially increasing the risk of infection.
Stryker is recalling Hoffmann LRF Safety Clips because they may loosen from the Quick Release mechanism on Transport Struts.
Cardinal Health 200, LLC is recalling specific lots of Jackson-Pratt Silicone Round Drains because the product seal may be compromised, potentially increasing the risk of infection.
Advanced Pharma Inc. is recalling all Diltiazem HCl products because they may contain latex but lack proper labeling.
Advanced Pharma Inc. is recalling Ropi/ Epi/ Clon PeriCapsular injection because the product may contain latex and lacks appropriate labeling.
Gentell, Inc. is recalling 65 gallons of Shield and Protect Moisture Barrier Cream because it may not meet cGMP requirements.
Advanced Pharma Inc. is recalling all lots of Dexmedetomidine HCl because the product may contain synthetic or natural latex, which is not currently labeled.
Advanced Pharma Inc. is recalling all Oxytocin products due to a labeling issue regarding potential synthetic or natural latex content.
Advanced Pharma Inc. is recalling Early TPN (Neonatal) products nationwide due to a labeling error regarding potential latex content.
Advanced Pharma Inc. is recalling all lots of Cefazolin because the product may contain latex but lacks appropriate labeling.