State
73,833 recalls have nationwide distribution and so reach Oklahoma. 5,824 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,824 recalls naming Oklahoma we have scored against our rubric, 1,040 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,494 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,824 recalls whose distribution notice names Oklahoma specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Stryker is recalling EliteCore Full Core Biopsy Devices because the cannula may extend past its intended length.
DePuy Orthopaedics is recalling 19,059 LCS COMPLETE RPS Femoral Implants because they are associated with higher revision rates and potential patello-femoral pain when the native patella is not resurfaced.
DePuy Orthopaedics is recalling LCS COMPLETE RPS knee inserts because they show higher revision rates in Australia when the patella is not resurfaced.
OptiMedica is recalling Catalys Precision Laser Systems with software version 3.00.05 because a software anomaly may provide incorrect cataract surgery parameters.
GE Healthcare is recalling D-Fend and D-Fend+ water traps because they may occlude, causing a loss of respiratory gas monitoring.
Medrad Inc dba Bayer R&I is recalling 133 Stellant CT Injector Systems with Certegra Workstations due to a configuration error that may cause under-infusion of contrast media.
Maquet Cardiovascular is recalling HLS/HIT Set Advanced consoles because a potential issue could cause blood to leak from the gas outlet port.
Terumo is recalling 1,713 Advanced Perfusion System 1 units worldwide due to a risk of losing system power during critical medical procedures.
Mindray is recalling four Panorama Patient Monitoring Network units due to a software anomaly that prevents arrhythmia alarms from displaying on the Panorama system after a restart.
Siemens is recalling 133 Luminos Agile Max imaging systems due to a software defect that causes image loss and connection issues.
Boehringer Ingelheim Roxane Inc is recalling Acarbose 50 mg tablets because potency was below specification at a 9-month stability time point.
Siemens is recalling 133 Axiom Luminos dRF Max imaging systems due to a software defect that can cause acquired images to be deleted, requiring studies to be repeated.
Siemens is recalling 75 SOMATOM Emotion 16 CT scanners due to software bugs that may cause system crashes, image freezes, or database locks, potentially requiring patients to be rescanned.
Siemens Medical Solutions is recalling 75 SOMATOM Emotion 6 CT scanners due to software bugs that may cause system crashes, image freezes, or database locks, potentially requiring patients to be rescanned.
Siemens is recalling 133 Ysio Max radiographic systems because a software defect can delete acquired images and studies, requiring patients to repeat exposures.
Siemens is recalling 133 Uroskop Omnia Max X-ray systems due to software defects that cause image deletion and connection issues.
Noven Pharmaceuticals is recalling 125,340 Daytrana patches because one lot exceeded the mechanical peel specification. The recall is nationwide.
Siemens is recalling 75 SOMATOM Perspective CT scanners due to software bugs that may cause system crashes, image freezes, or database locks, potentially requiring patients to be rescanned.
Biocare Medical is recalling 19 units of D2-40 Lymphatic Marker because incorrect Instructions for Use were shipped with the product.
Teva Pharmaceuticals is recalling QVAR inhalers because stability testing revealed out-of-specification impurity results.
Ubervita LLC is recalling less than 30 units of W700 Lose Weight Fast W700 Thermogenic Hyper-Metabolizer dietary supplements sold at Walmart due to a packaging error.
Ford is recalling 2015 Mustangs with 2.3L engines because heat can degrade fuel lines, causing leaks and fire risks.
Mitsubishi is recalling 2006-2009 Eclipse and 2007-2009 Eclipse Spyder vehicles because corrosion in the ABS unit may cause valves to seize, reducing braking ability.
Airstream is recalling 2015-2016 Interstate NCV3 B motorhomes because the screen door may prevent occupants from opening the sliding door to exit in an emergency.
Mitsubishi, Chrysler, and Dodge are recalling specific 2000-2005 vehicles because the passenger sun visor may detach during airbag deployment, increasing injury risk.