State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Hyundai is recalling 2011-2015 Sonata and Sonata Hybrid vehicles previously repaired under a prior campaign because seat belt linkages may detach from pretensioners, increasing injury risk in a crash.
Sorin Group is recalling Platinium VR implantable cardioverter defibrillators due to a possibility of overconsumption following electrostatic discharge or MRI scans.
Zimmer Biomet is recalling 62 ECT Internal Fracture Fixation Quick-Connect Drills because raw material anomalies may cause the instruments to fracture during use.
Toyota is recalling 2010 Lexus HS 250h Hybrid vehicles because a hybrid transaxle component may short circuit, causing a loss of power and increasing crash risk.
Zimmer Biomet is recalling specific orthopedic drill bits and screw taps because raw material anomalies may cause the instruments to fracture during use.
Zimmer Biomet is recalling 10 units of ECT Internal Fracture Fixation Quick-Connect Drills due to a raw material anomaly that may increase the risk of instrument fracture during use.
Zimmer Biomet is recalling 185 NCB Periprosthetic Plate System Drill Bits due to a raw material anomaly that may increase the risk of instrument fracture during use.
Grand Design RV is recalling 2017-2018 Imagine recreational trailers because air conditioning wires may detach and short circuit, increasing fire risk.
Zimmer Biomet is recalling 4 units of ECT Internal Fracture Fixation Quick-Connect Drills due to raw material anomalies that may increase the risk of instrument fracture.
Zimmer Biomet is recalling 198 nonsterile orthopedic screw taps because raw material anomalies may increase the risk of instrument fracture during use.
Zimmer Biomet is recalling 21 units of M/DN Intramedullary Fixation Femoral Drills because raw material anomalies may cause the instruments to fracture during use.
Zimmer Biomet is recalling 1,091 nonsterile orthopedic surgical drills and screw taps because raw material anomalies may cause instrument fracture.
Zimmer Biomet is recalling specific orthopedic drill bits and screw taps because a raw material anomaly may increase the risk of instrument fracture during use.
Teleflex Medical is recalling Percuvance 29cm Shaft surgical systems because the shaft connection may be compromised or tool tips may close abruptly.
Zimmer Biomet is recalling 1,999 ECT Internal Fracture Fixation Drills because raw material anomalies may increase the risk of instrument fracture during use.
Teleflex Medical is recalling Percuvance Johans Grasper Tool Tips because the shaft connection may be compromised or the jaws may close abruptly.
Zimmer Biomet is recalling 453 nonsterile orthopedic drill bits because raw material anomalies may cause instrument fracture during use.
Teleflex Medical is recalling 20,039 Percuvance Clip Applier Tool Tips because the shaft connection may be compromised or the jaws may close abruptly.
Transportation Collaborative is recalling 2015-2016 Trans Tech school buses because seat mounting studs lack adequate padding, increasing injury risk in rear-end collisions.
Zimmer Biomet is recalling 10 units of ECT Internal Fracture Fixation Long Drills due to raw material anomalies that may increase the risk of instrument fracture.
Zimmer Biomet is recalling 1,255 ECT Internal Fracture Fixation Drill Bits due to raw material anomalies that may increase the risk of instrument fracture during use.
Zimmer Biomet is recalling 25 units of M/DN Intramedullary Fixation Femoral Drills due to raw material anomalies that may increase the risk of instrument fracture during use.
Zimmer Biomet is recalling specific orthopedic drill bits and screw taps because raw material anomalies may increase the risk of instrument fracture during use.
Zimmer Biomet is recalling 173 orthopedic surgical instruments because a material anomaly may increase the risk of instrument fracture during use.
Zimmer Biomet is recalling 705 nonsterile orthopedic drill bits and screw taps because raw material anomalies may cause instrument fracture during use.