State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The Harvard Drug Group is voluntarily recalling Major Poly-Vita Drops due to possible B. cepacia contamination, which poses a serious infection risk to immunocompromised patients.
Bella Pharmaceuticals is recalling 200 prefilled BevaDex syringes nationwide because the company cannot guarantee the product's sterility.
Navistar is recalling 2016 IC Bus CE school buses because a steering component may loosen, potentially causing a loss of steering and increasing crash risk.
Bella Pharmaceuticals is recalling 45 vials of B-Complex due to a lack of assurance of sterility. The affected lot is BPBC3080517, expiring 2/5/18.
Centurion Labs is recalling Ninjacof-A oral solution due to potential B. cepacia contamination. Consumers should stop using the product and return it to the pharmacy.
The Harvard Drug Group is voluntarily recalling Rugby Tri-vitamin Liquid due to possible contamination with B. cepacia, which poses a risk of serious infection for vulnerable patients.
The Harvard Drug Group is voluntarily recalling Major Ferrous Drops due to possible B. cepacia contamination, which poses a serious infection risk to vulnerable patients.
Bella Pharmaceuticals is recalling 2,334 Bevacizumab prefilled syringes nationwide due to a lack of assurance of sterility.
The Harvard Drug Group is voluntarily recalling Major Poly-Vita Drops with Iron due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.
Bella Pharmaceuticals is recalling Mannitol 20% 10 mL vials because the company cannot ensure the product is sterile.
Volkswagen is recalling 2004-2007 Touareg vehicles because a fuel filter flange may crack, causing a fuel leak that increases the risk of fire.
The Harvard Drug Group is voluntarily recalling Rugby Calcionate Syrup due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.
Zydus Pharmaceuticals is recalling 44,800 bottles of 30mg Paroxetine tablets because foreign Risperidone tablets were found in the packaging.
The Harvard Drug Group is voluntarily recalling Rugby Ferrous Sulfate Liquid due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.
Bella Pharmaceuticals is recalling 7 vials of Methylcobalamin 10mg due to a lack of assurance of sterility. The product was distributed nationwide in the United States.
Leader Liquid Vitamin D Supplement for Breastfed Infants is being voluntarily recalled due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.
Bella Pharmaceuticals is recalling Magnesium Chloride 200mg vials because the company cannot ensure the product is sterile.
Bella Pharmaceuticals is recalling specific lots of Calcium chloride 10% vials because the company cannot ensure the product is sterile.
The Harvard Drug Group is voluntarily recalling Rugby Cerovite Liquid due to possible B. cepacia contamination, which may cause serious infections in vulnerable patients.
The Harvard Drug Group is voluntarily recalling Rugby D 3 Vitamin Liquid due to possible B. cepacia contamination, which poses a serious infection risk to vulnerable patients.
Porsche is recalling specific 2003-2006 Cayenne models because a fuel pump flange may crack, allowing fuel to leak and increasing fire risk.
Bella Pharmaceuticals is recalling specific lots of L-Glutamine 100mg vials because the company cannot guarantee the product is sterile.
Double K is recalling 2016-2017 Hometown Trolley buses because the seat belt buckle may be stuck in the locked position, preventing the belt from latching.
DEMDACO is recalling about 1,500 infant bib and bootie sets because rattle attachments can detach, posing a choking hazard. No injuries have been reported.
Zimmer Biomet is recalling 64 ROSA surgical device foot switches that may freeze or shut down during use.