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.
Simply Delicious, Inc. is recalling Bobo's Coconut Oat Bars because they may contain mold. The recall covers 588 master cases distributed nationwide.
Angiodynamics, Inc. is recalling Accu2i pMTA Microwave Tissue Ablation Applicators because coolant ingress may prevent the device from delivering desired microwave energy.
Zimmer Biomet is recalling 7,888 Humeral Guide Wire Ball Tip units because the previous packaging configuration lacks design verification for 70cm wires.
G & W Laboratories is recalling 142,236 tubes of Ciclopirox Olamine Cream USP, 0.77%, due to yellow discoloration. The product is distributed nationwide and in Puerto Rico.
Teva Pharmaceuticals is recalling Fentanyl Transdermal Systems because a degradation product exceeded safety limits.
Teva Pharmaceuticals is recalling specific lots of Fentanyl Transdermal Systems because a degradation product exceeded safety limits.
West Elm is recalling Jensen rectangular glass tables because the tempered glass tops can shatter unexpectedly, posing a laceration hazard.
Tea Collection is recalling about 3,800 children's rompers because snaps near the collar can detach, posing a choking hazard to young children.
Gulf Stream is recalling 2018 Matrix and Geo recreational trailers because the Federal Certification Labels incorrectly list the rear axle weight rating.
Ford is recalling 2018 Escape and Lincoln MKC vehicles because incorrect front brake hoses may chafe and leak fluid, increasing stopping distance.
Mitsubishi is recalling 2011-2016 Outlander Sport vehicles because water intrusion may corrode the wiper link, causing wipers to stop working and reducing visibility.
Volkswagen is recalling 2017-2018 Tiguan Limited vehicles because the front driver air bag may not be intended for US use, failing federal safety standards and increasing injury risk in a crash.
Fujitsu is recalling specific lithium-ion battery packs for notebook computers and workstations because they can overheat, posing fire and burn risks.
Micro Bird is recalling 2015-2018 T-Series transit buses because seat belt attachments may not remain secured to the floor in a crash, increasing injury risk.
Poppin is recalling about 2,800 Pitch rolling chairs because the seat plate can break and detach, posing a fall hazard. No injuries have been reported.
Chrysler is recalling 2017 Jeep Wrangler and Dodge Caravan vehicles because brake switches may malfunction, allowing the vehicle to shift out of Park without the brake pedal being pressed.
BMW is recalling 2018 Rolls-Royce Ghost vehicles because head air bags may not fully inflate during a crash, increasing injury risk.
Halcore Group is recalling 2017 AEV Traumahawk ambulances because a battery isolator module may overheat, posing a fire and injury risk.
Husqvarna is recalling about 7,100 residential zero turn riding mowers because a fuel line defect can cause leaks and fire. No injuries have been reported.
Chrysler is recalling 2017-2018 RAM trucks because the brake pedal interlock may fail, allowing the vehicle to shift out of Park without the brake pedal being pressed.
Blue Fusion Natural is recalling Blue Pearl capsules because FDA analysis found undeclared sildenafil, an unapproved drug for erectile dysfunction.
International Laboratories, LLC is recalling Clopidogrel Tablets 75 mg because bottles were found containing Simvastatin Tablets 10 mg.
Medline is recalling Incision and Drainage Tray Kits because the Povidone-Iodine prep pads contain less iodine than labeled.
Medline Industries is recalling 60 cases of Anesthesia Kits because the Povidone-Iodine prep pads contain less iodine than the label claims.
Medline Industries is recalling Suture Removal Kits because the iodine concentration is below the label claim.