State
73,741 recalls have nationwide distribution and so reach Oklahoma. 5,822 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,822 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 1,493 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,822 recalls whose distribution notice names Oklahoma specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Keystone is recalling 2019 Summerland recreational trailers because the Federal Identification Label lists an incorrect tire rim size, which could lead to improper rim replacement.
Spartan Motors is recalling 2009-2018 Gladiator and MetroStar emergency vehicles because internal corrosion in the fire water pump solenoid may cause loss of water pressure, increasing injury risk.
Mazda is recalling 2018 CX-5 vehicles because side curtain air bags may not unfold properly in a crash, increasing injury risk.
Volkswagen Group of America is recalling specific Audi models because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
REV is recalling 2019 Fleetwood Flair and Holiday Rambler Admiral motorhomes because non-flexible wiring in the bedroom slide-out may damage and cause a fire.
E-One is recalling 2016-2017 Cyclone II emergency vehicles because stress fractures in the aerial ladder tubing could cause failure and injure the bucket occupant.
Triple E RV is recalling 2017-2018 Wonder recreational vehicles because water can corrode wiring in the trailer tow module, potentially causing electrical shorts, fire, or crash risks.
Ricon is recalling S-Series and K-Series wheelchair lifts because a component may fail, allowing the platform to rise too high and increase injury risk.
Achieva Rubber Corp. is recalling specific Innova Ultra Runner tires that fail to meet Federal Motor Vehicle Safety Standard 119, posing a crash risk.
BMW is recalling 2018 X3 xDrive30i and M40i vehicles because rear turn signals may display incorrect colors, potentially confusing other drivers.
Syncro is recalling Hayes Sway Master units that may disable trailer brakes, increasing crash risk.
Inopak Ltd is recalling Option Systems Antibacterial Foaming Hand Wash because FDA analysis found out-of-specification microbial counts.
Angiodynamics Inc. is recalling 13 boxes of RS Tandem 5F DL Xcela PICC catheters because a component may contain unsafe levels of bacterial endotoxins.
TRW is recalling air bag control units in certain Hyundai and Kia vehicles because electrical overstress may prevent air bags and seat belt pretensioners from deploying in a crash.
Angiodynamics Inc. is recalling 2 boxes of CAN 5F DL BIOFLO PASV PICC Nursing Trays because a component may contain unsafe levels of bacterial endotoxins.
Angiodynamics Inc. is recalling 5F DL BIOFLO PICC kits because a component may contain unsafe levels of bacterial endotoxins.
Angiodynamics Inc. is recalling 17 boxes of CAN 5F SINGLE XCELA PICC kits because a component may contain unsafe levels of bacterial endotoxins.
Angiodynamics Inc. is recalling 3 boxes of RS - TANDEM 5F DL BIOFLO MIDLINE catheters because a component may contain unsafe levels of bacterial endotoxins.
Angiodynamics Inc. is recalling 298 boxes of Bio-Stable 5F kits because a component may contain unsafe levels of bacterial endotoxins.
Shadow Holdings DBA Bocchi Labs is recalling the Acne Shave 3 Step Shaving System due to CGMP deviations that may result in bacterial contamination.
Medline Industries is recalling specific lots of READYFLUSH PROTECT flushable personal cleaning cloths because of microbial contamination in a non-sterile product.
Allergan is recalling Taytulla softgel capsules because the tablets are out of sequence. This affects 168,768 blister cards distributed nationwide.
Angiodynamics Inc. is recalling 17 boxes of Bio-Stable 5F kits because a component may contain unsafe levels of bacterial endotoxins.
Angiodynamics Inc. is recalling BioFlo PICC nursing kits because a component may contain unsafe levels of bacterial endotoxins.
Angiodynamics Inc. is recalling RS 5F DL XPP kits because a component may contain unsafe levels of bacterial endotoxins.