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.
Stork Craft is recalling about 18,500 foam crib mattresses because they fail to meet federal flammability standards, posing a fire hazard.
Nipponflex is recalling about 400 Smart Flex and Smart Care mattresses because they fail to meet federal flammability standards, posing a fire hazard.
Forest River is recalling 160 motorhomes because the back-up camera system may display reversed images, increasing the risk of a crash.
Liftmoore is recalling 2001-2006 6036WX truck cranes because a specific battery equalizer part may conduct electricity when heated, increasing fire risk.
Forest River is recalling 2014-2016 Sandpiper and Sierra recreational vehicles because inaccurate gross vehicle weight rating labels could mislead owners about capacity.
ACCO Brands is recalling about 3.3 million Quartet magnetic and dry erase boards because sharp metal edges on the back can cause lacerations when removing the boards.
Heartland is recalling various trailer models because tire certification labels may contain inaccurate sizing or inflation information, potentially leading to tire failure.
Western / Scott Fetzer Company is recalling OxyTOTE Portable Oxygen System regulators due to a risk of ignition and rupture of the oxygen cylinder.
American Medical Systems is recalling 16,710 Sureflex 910 Lithotripsy Fibers because cleaning and sterilization validation data do not meet FDA guidance for reusable products.
American Medical Systems is recalling 16,710 Fiber Stripper tools because cleaning and sterilization validation data do not meet FDA guidance for reusable products.
Philips is recalling 13 GEMINI TF 16 Slice CT/PET systems worldwide due to four software defects in the Tumor LOC application that may affect treatment accuracy.
Philips is recalling 22 GEMINI TF 64 Slice CT/PET systems due to software defects that may cause incorrect tissue irradiation.
Philips is recalling two Gemini LXL CT/PET systems due to software defects that may cause incorrect radiation delivery to patients.
The FDA is recalling 5,786 sterile Double Basin Kits because the included Devon Light Gloves contain splits or holes that compromise sterility.
DePuy Orthopaedics is recalling ATTUNE FB PS Articulation Surface instruments because a small wire spring coil (Balseal) may detach and be left in the patient during surgery.
Philips is recalling two GEMINI TF Base CT/PET systems because four software defects in the Tumor LOC application may cause incorrect tissue irradiation.
The FDA is recalling 4,136 sterile surgical kits because the Devon Light Gloves inside contain splits or holes that compromise sterility.
American Medical Systems is recalling Sureflex 150 Lithotripsy Fibers because cleaning and sterilization validation data do not meet FDA guidance for reusable medical devices.
FDA is recalling 33,256 surgical set up kits containing Devon Light Gloves that have splits or holes compromising sterility.
Philips is recalling GEMINI TF Ready CT/PET systems due to software defects that may cause incorrect radiation treatment.
Whirlpool is recalling Jenn-Air wall ovens because the extendable roller rack can unexpectedly disengage, posing a burn risk. Consumers should stop using the rack and contact Whirlpool for a free repair.
American Medical Systems is recalling Fiber Stripper tools because cleaning and sterilization validation data do not meet FDA guidance for reusable products.
DePuy Orthopaedics is recalling ATTUNE Knee Tibial Articulation Surface Instruments because a small wire spring coil may detach and be left in patients during surgery.
Volcano Corporation is recalling s5/s5i/CORE Intravascular Ultrasound Systems due to a software issue that may calculate inaccurate FFR/iFR values.
The FDA is recalling 144 sterile Augmentation Kits containing Devon Light Gloves due to splits or holes that compromise sterility. The affected kits were distributed worldwide.