State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ortho-Clinical Diagnostics is recalling 30 enGen Laboratory Automation Systems due to a software error that displays incorrect interpretive text for certain test results.
Ortho Clinical Diagnostics is recalling specific lots of VITROS AFP Reagent Packs because they may fail to calibrate, potentially affecting test results.
Apotex Scientific is recalling specific lots of Duloxetine Delayed-Release Capsules because they failed dissolution specifications during stability testing.
West-Ward Columbus Inc. is recalling 1,182 bottles of Oxycodone Hydrochloride Oral Solution due to failed impurities and degradation specifications.
Blue Bird is recalling 2016-2017 Vision transit buses with 6.8L Ford engines and Gen 3 propane units because fuel lines may rub, causing leaks and fire risk.
Charles Machine Works is recalling 2016 Ditch Witch T14MV trailers because an incorrect wiring harness may prevent brakes from applying if the trailer separates from the tow vehicle.
Blue Bird is recalling 2,902 school buses due to propane fuel lines that may rub and leak, increasing the risk of fire.
BMW is recalling 956 model year 2015 M5 and M6 vehicles because a defective driveshaft weld may cause loss of propulsion or vehicle rolling, increasing crash risk.
Spartan Motors is recalling 2011-2015 Transit Bus Chassis Cabs because frames may crack, potentially reducing driver control and increasing crash risk.
Bar-S Foods is recalling approximately 372,684 pounds of chicken and pork hot dog and corn dog products due to possible Listeria monocytogenes contamination.
Bentley is recalling 2007-2009 Continental Flying Spur vehicles because the sunroof glass may not be properly secured and could detach while driving.
GSI Outdoors is recalling about 6,700 children's insulated water bottles sold at L.L.Bean because lead solder at the base violates safety standards.
Starcraft RV is recalling 2016-2017 AR-ONE Maxx travel trailers and fifth wheels because incorrect tire labels may lead to improper tire replacement.
Things Remembered is recalling silver bracelets and charm necklaces for children because the clear surface coating contains lead in excess of allowable limits.
ConAgra Foods is recalling approximately 195,597 pounds of frozen P.F. Chang's Home Menu chicken and beef products due to potential metal contamination. No injuries have been reported.
Nestlé Waters North America is recalling AccuPure countertop water dispensers because they can overheat, melt, and smoke, posing fire and burn risks.
Flushmate is recalling about 453,000 Flushmate III Pressure-Assist Flushing Systems in the U.S. because the units can burst, posing impact and laceration hazards.
Home Source is recalling about 2,700 floor lamps sold in the New York area and online because defective sockets can cause fires and electric shocks.
Altec is recalling 252 model year 2015-2016 Aerial Devices and Digger Derricks because a hydraulic motor shaft may fail, causing unexpected winch movement and increasing injury risk.
IKEA is recalling PATRULL safety gates and extensions because the locking mechanism can open unexpectedly, posing a fall hazard to children.
The Clorox Company is recalling three Liquid Plumr clog remover products because the bottles lack required child-resistant closures, posing a risk of chemical burns.
Haring Catfish, Inc. is recalling approximately 21,521 pounds of catfish products found to contain gentian violet, a chemical residue of public health concern.
Bee Extremely Amazed LLC is recalling XCEL Capsules marketed as a dietary supplement because they contain undeclared fluoxetine and phenolphthalein.
Bee Extremely Amazed LLC is recalling Prime Capsules because they contain undeclared sibutramine and phenolphthalein, making them unapproved drugs.
Bee Extremely Amazed LLC is recalling Oasis Capsules because they contain undeclared sibutramine and phenolphthalein, making them unapproved drugs.