State
73,827 recalls have nationwide distribution and so reach Oklahoma. 5,823 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,823 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 5,823 recalls whose distribution notice names Oklahoma specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Z Gallerie is recalling Golda wall clocks because defective battery springs can cause batteries to overheat, posing a fire hazard.
Philips Medical Systems is recalling 677 BrightView gamma cameras because the collimator may contact the patient pallet or the gantry may halt prematurely during scans.
Aesculap Inc. is recalling 1,232 units of Columbus Revision and EnduRo Knee System packaging labeled as cementless, which are indicated for use with bone cement only.
Sun Pharma Global Fze is recalling specific lots of Alendronate Sodium Tablets 70 mg because unknown impurity levels exceeded specifications during stability testing.
Novadaq is recalling 110 PINPOINT Endoscopic Fluorescence Imaging Systems because the operator's manual lacks validated sterilization parameters for specific components.
Stryker is recalling AccuPlace Drace Stereotaxic Needle Guides because packaging defects may breach sterility. The recall covers 5,800 units distributed nationwide.
Stryker is recalling AccuPlace Round Level Needle Guides because packaging defects may compromise sterility. The recall affects 5,800 units distributed nationwide.
Volcano Corporation is recalling R-100 Sterile Equipment Covers because the outer shipping boxes may display incorrect expiry dates, although the inner product is correctly labeled.
Stryker is recalling AccuPlace Straight Level Needle Guides because packaging defects may compromise sterility. The recall affects 5,800 units distributed nationwide.
Medical Action Industries is recalling 180 PICC/CVC Secure Dressing Change kits because the presence of CHG is not identified on the exterior labeling.
Stryker is recalling 5,800 AccuPlace Drace Stereotaxic Needle Guides due to a potential breach in sterility caused by packaging damage.
Volcano Corporation is recalling certain lots of R-100 Sterile Equipment Covers because the outer shipping boxes may display incorrect expiry dates, although the inner product is correctly labeled.
Teva North America is recalling 1,895 bottles of Capecitabine tablets because they failed dissolution specifications at the 18-month time point.
Zimmer Spine is issuing a Class II correction for the Virage OCT Spinal Fixation System to provide additional guidance in the surgical technique manual.
J. Strickland and Co is recalling Sulfur8 Medicated Light Formula anti-dandruff conditioner because it failed stability testing. The product is subpotent.
Setra is recalling 2005-2009 S417 coaches because a cracked control arm tube can separate, potentially causing loss of vehicle control and increasing crash risk.
Spartan Motors is recalling 2014-2015 Gladiator and MetroStar emergency vehicles because a faulty sensor may incorrectly display the fire-suppression agent level.
Liberty Hardware is recalling about 374,000 decorative metal wall plates because they can dislodge and short circuit outlets, posing electrical shock and fire hazards.
Navistar is recalling specific 2016-2017 International trucks and 2016 IC buses because a parking brake cable clip may fail, causing the vehicle to roll unexpectedly.
Thor Motor Coach is recalling 385 model year 2014-2016 Hurricane and Windsport motor homes because heat from the exhaust system may cause a storage compartment to melt, increasing the risk of fire.
ZF Group is recalling specific front control arms where a manufacturing defect may cause the tube to separate from the shaft, potentially leading to loss of vehicle control.
Volkswagen is recalling 2015-2016 e-Golf vehicles because oversensitive battery diagnostics may cause the electric motor to shut down unexpectedly, increasing crash risk.
USDA FSIS issued a public health alert for Yummy brand chicken nuggets potentially contaminated with metal pieces. No illnesses have been reported.
Jaguar is recalling 2013-2015 XF vehicles because a faulty engine component may cause a loss of power steering assist, increasing crash risk.
Prevost is recalling 2015-2016 X3-45 buses because cracks in sliding passenger seats may compromise structural integrity, increasing injury risk in crashes.