State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Salewa North America is recalling Wild Country Syncro climbing harnesses because excess materials on the waist belt tab can cause the harness to loosen, posing a fall hazard.
Montana Flour & Grains is recalling 100% Organic Spelt Grain because the label fails to declare wheat, a major allergen.
Talon Compounding Pharmacy is recalling 6,500 vials of Human Chorionic Gonadotropin Injection nationwide due to a lack of assurance of sterility.
Conmed is recalling Adult ThermoGard Dual Dispersive Electrodes because they may be incompatible with some electrosurgical generators, posing a risk of undetected pad lift and potential burns.
Daimler Trucks is recalling 2015-2017 Thomas Built Buses equipped with certain Ricon wheelchair lifts because pivot holes may allow bearings to move, risking platform failure.
PACCAR is recalling one 2017 Peterbilt 567 truck because a bracket protrudes upward, creating a tripping hazard. Dealers will move the connections to the right rail free of charge.
Bovie Medical Corporation is recalling 95 units of the BVX-450BR Bovie Precise 360 Handpiece because the adhesive bond to the angled tip may be incomplete.
Daimler Trucks North America is recalling 2015-2017 Thomas Built Buses equipped with specific Ricon wheelchair lifts. Defective pivot holes may allow bearings to move, causing the lift platform to fall and injure the operator.
Hyundai is recalling 2007-2008 Azera vehicles because the driver's power seat may move unexpectedly, increasing crash risk.
Montana Flour & Grains, Inc. is recalling 100% Organic Unbleached White Flour because the label does not declare wheat, a major food allergen.
Swarovski is recalling Octa Crystal Pendant light fixtures because the crystal can detach and fall if damaged during shipment, posing an impact hazard.
Montana Flour & Grains is recalling 100% Organic Spelt Flour because the label does not declare wheat, a major food allergen.
Mondelez International is recalling Nabisco Honey Maid Teddy Grahams Cinnamon Cubs because they were produced using flour containing peanut residue.
Philips is recalling 30 Ingenuity Core CT systems because a software upgrade can cause planned anatomy to be cut off in gated helical scans.
Conmed Corporation is recalling Adult Dual Dispersive Electrodes because they may be incompatible with some electrosurgical generators, creating a risk of undetected pad lift and potential burns.
GE OEC Medical Systems is recalling 47 OEC UroView 2800 fluoroscopic x-ray systems because a firmware issue may cause the LCD workstation monitor to appear dark with no video displayed.
GE OEC Medical Systems is recalling 47 OEC 9800 fluoroscopic x-ray systems because a firmware issue may cause the LCD workstation monitors to appear dark with no video displayed.
Teva North America is recalling Amoxicillin for Oral Suspension because stability testing showed the drug was superpotent.
Philips is recalling 50 Brilliance CT 16 Power systems due to a software defect that may cause planned anatomy to be cut off in images, potentially requiring a rescan.
Philips Medical Systems is recalling 192 Brilliance 16 CT scanners because a software upgrade can cause planned anatomy to be cut off in images, potentially requiring a rescan.
Philips is recalling 33 Brilliance CT Big Bore Oncology systems due to a software defect that may cause planned anatomy to be cut off in gated helical CT images.
Philips is recalling 283 Brilliance 64 CT scanners because a software update can cause planned anatomy to be cut off in images, potentially requiring a rescan.
Novarad Corporation is recalling NovaPACS software versions 8.4.7, 8.5.3, and 8.5.6 due to a prematurely released pop-up screen.
Merz North America is recalling 1,591 units of Radiesse (+) Lidocaine Injectable Implant because the product could not be expelled from the syringe or needle.
Integra LifeSciences is recalling QWIX Compression Screws because the product labeling incorrectly identifies them as compression screws rather than positioning screws.