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.
Bausch & Lomb is recalling Algerbrush-II surgical instruments because some units shipped with outdated operating instructions.
Siemens is recalling 41 Biograph mCT PET/CT scanners because laser cover windows may fall off.
Siemens Medical Solutions is recalling 18 Biograph mCT X-3R scanners because laser cover windows may fall off.
Willow Tree Poultry Farm is recalling 204 pounds of chicken salad products because they are misbranded as chicken salad but contain egg salad.
Pfizer is recalling 1,706 cartons of Cytotec (misoprostol) tablets nationwide because the product failed impurity and degradation specifications.
4-Star Trailers is recalling 2012-2016 Gooseneck Horse trailers because a hydraulic brake line may rupture, causing a loss of braking power and increasing crash risk.
Highland Ridge RV is recalling 2017 Open Range, Mesa Ridge, and Roamer models because the outside range can be stored with the gas valve open, creating a fire or explosion hazard.
RH Baby & Child is recalling vintage race car mobiles because wheels can detach and fall, posing a choking hazard to young children.
Triumph is recalling 2016-2017 Bonneville T100 motorcycles because heated hand grips may expand and cause the throttle to stick open, increasing crash risk.
REV Recreation Group is recalling specific Renegade RV motorhomes because seat belt anchorage hardware may pull out of the floor framing during a crash.
Nantucket Distributing is recalling pre-lit artificial Christmas trees because the fuse can overheat and blow, posing a fire hazard. No injuries have been reported.
BRP is recalling about 780 Can-Am Defender side-by-side off-road vehicles because they can unexpectedly roll away while in park, posing an injury risk.
General Motors is recalling 2016-2017 Chevrolet Suburban HD vehicles equipped with a convex right-hand outside mirror instead of a non-convex one, which may cause drivers to misjudge distance.
Yamaha is recalling about 400 model year 2016 SR10 SRViper snowmobiles equipped with dealer-installed MPI Turbo Kits because turbocharger overboost can cause severe engine damage, posing crash and fire hazards.
Boosted Inc. is recalling 2nd Generation Dual+ electric skateboards because the lithium ion battery packs can overheat and smoke, posing a fire hazard.
Textron Specialized Vehicles is recalling about 1,100 Bad Boy off-road utility vehicles because they lack seat belts, posing a risk of serious injury or death.
Wells Pharmacy Network LLC is recalling 265 vials of compounded Methylcobalamin 5,000 mcg/mL Injectable because the product lacks assurance of sterility.
Tri-Coast Pharmacy is recalling 1,304 vials of compounded HCG/Hydroxycobalamin nationwide due to a lack of assurance of sterility.
Wells Pharmacy Network LLC is recalling 46 kits of compounded Ceftazidime Ophthalmic 2.25% due to a lack of assurance of sterility.
Tri-Coast Pharmacy is recalling 2 units of TriMix injection because the agency cannot assure the products are sterile.
Tri-Coast Pharmacy is recalling 50 vials of compounded L-Tyrosine 10 mg/mL because the products lack assurance of sterility.
Wells Pharmacy Network LLC is recalling 335 vials of Vitamin D3 in Sesame Oil Injectable due to a lack of assurance of sterility.
Tri-Coast Pharmacy is recalling 920 vials of compounded Sermorelin GT nationwide due to a lack of assurance of sterility.
Tri-Coast Pharmacy is recalling 41 vials of compounded L-Arginine HCL 100 mg/mL because there is a lack of assurance of sterility. The products were distributed nationwide.
Tri-Coast Pharmacy is recalling 260 vials of Sermorelin Acetate 6 mg compounded between May and November 2016 because the agency cannot assure the products are sterile.