State
73,833 recalls have nationwide distribution and so reach Oklahoma. 5,824 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,824 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 5,824 recalls whose distribution notice names Oklahoma specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Northern Tool + Equipment is recalling Little Digger Toys because the red paint contains excessive lead levels prohibited by federal law.
lululemon athletica is recalling about 133,000 women's tops in the U.S. because elastic draw cords can snap back and injure the face or eyes.
AstraZeneca is recalling NEXIUM capsules because a retail pharmacist found SEROQUEL XR tablets in an unopened bottle.
Shred-Tech is recalling specific MDS models because EPA emission controls cause the front axle to exceed its certified weight rating, increasing crash risk.
Whole Foods Market is recalling Muffin Bran 6Pk packages due to undeclared milk and eggs. Consumers should check their pantries for affected products.
Cruiser RV is recalling 2016 Stryker travel trailers because wheel studs may break, potentially causing the wheel to detach and increasing crash risk.
SR Suntour is recalling bicycles with specific fork models because a bolt can break, causing the front wheel to detach. This poses a crash hazard to riders.
Beaver-Visitec International is recalling 621 ophthalmic procedure kits because the included Devon Light Glove may have holes or slits that compromise sterility.
Positec Tool Corp. is recalling Worx electric blower/vacs because reversed wiring poses a shock hazard. No injuries have been reported.
Stryker is recalling 72 Navigation System II-Carts because a weld seam defect may cause the articulated arm joint to fail.
Beaver-Visitec International Inc. is recalling 268 ophthalmic procedure kits because the included Devon Light Gloves may have holes or slits that compromise sterility.
Smiths Medical is recalling CADD-Solis Ambulatory Infusion Pumps because the locking assembly may bind, preventing the cassette or keypad from locking securely.
Beaver-Visitec International is recalling 585 ophthalmic procedure kits because the Devon Light Glove component may have holes or slits that compromise sterility.
Synthes, Inc. is recalling Pull Reduction Devices for 4.3mm Percutaneous Drill Guides because incorrect hardness specifications may cause the devices to break during surgery.
Integra LifeSciences is recalling Camino Intracranial Pressure Monitoring Catheters because incorrect assembly may allow cerebrospinal fluid or blood to leak.
CareFusion 303, Inc. is recalling 63 Alaris PC unit model 8015 infusion pumps due to a software defect that may allow infusions to start outside hospital-established limits.
Beaver-Visitec is recalling 384 ophthalmic procedure kits because the included Devon Light Gloves may have holes or slits that compromise sterility.
School Specialty is recalling about 1,350 NeoRok stools because they can break during use, posing a fall hazard. No injuries have been reported.
Philips is recalling Q-Station ultrasound software because patient measurements may be incorrectly appended to other patients' studies.
Beaver-Visitec is recalling 214 ophthalmic procedure kits because the included Devon Light Gloves may have holes or slits that compromise sterility.
Dannmar is recalling MaxJax Portable Two-Post automatic car lift systems due to insufficient welding on lower carriage plates, which could cause the lift arms to snap and the vehicle to fall.
Roadtrek is recalling 335 model year 2014 motorhomes because electrical wiring under the front seats may damage, preventing the optional front thorax air bags from deploying in a crash.
Spartan Motors is recalling 2010-2015 Furion, Gladiator, and Metrostar emergency vehicles because the engine cooling fan may crack and detach, posing an injury risk to nearby individuals.
Neuro Kinetics is recalling 140 I-Portal NOTC and VNG devices due to system malfunctions and unintended sudden movements at startup. No injuries have been reported.
Ford is recalling 2014-2015 Escape and Transit Connect vehicles because a software issue may cause the instrument panel to stop working, potentially hiding safety warnings.