State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Stryker Howmedica Osteonics Corp. is recalling Gamma K-Wires because a packaging review found that the seal integrity of the pouch may be decreased.
Stryker Howmedica Osteonics Corp. is recalling T2 Guidewires because a packaging review found that the seal integrity of the pouch may be decreased.
Zimmer Biomet is recalling CPT 12/14 COCR hip prostheses because the LDPE packaging bag adheres to the polished implant surface.
Stryker Howmedica Osteonics Corp. is recalling T2 K-Wires because a packaging review found that the seal integrity of the pouch may be decreased.
Stryker Howmedica Osteonics Corp. is recalling T2 Guidewires because a packaging review found that the seal integrity of the pouch may be decreased.
Bigwall Enterprises is recalling WARM STEAM Personal Steam Inhalers nationwide due to unconfirmed consumer complaints. No causal link to product use has been established.
Stryker is recalling T2 K-Wires because the packaging seal integrity may be decreased, potentially affecting the sterility of the medical devices.
Zimmer Biomet is recalling 289 CPT 12/14 COCR hip prostheses because the LDPE packaging bag adheres to the implant surface.
Zimmer Biomet is recalling 194 Metasul Head 40 total hip prosthesis components because the packaging bag adheres to the implant surface.
Fresenius Medical Care is recalling Naturalyte Liquid Acid Concentrate because the label incorrectly lists the calcium concentration.
Zimmer Biomet is recalling 101 Versus 7.5 inch hip prostheses because the LDPE packaging bag adheres to the implant surface.
Olympus Scientific Solutions Americas is recalling Delta XRF Analyzers because the firm discovered a software bug.
Zimmer Biomet is recalling NexGen Knee CR femoral components because the packaging bag adheres to the implant surface.
Becton, Dickinson and Company is recalling 78 units of BD FMC7 FITC reagent because the vial labels display an incorrect expiration date.
Hospira is recalling 10,778 bags of Normosol-M and 5% Dextrose Injection due to an incorrect expiration date printed on the primary container.
Zimmer Biomet is recalling CR Flex and LPS Flex knee prostheses because the LDPE packaging bag adheres to the polished implant surface.
Isomeric Pharmacy Solution, LLC is recalling 114 vials of Triamcinolone Diacetate Injectable Suspension because some vials may have incorrect lot numbers or expiration dates.
Maserati is recalling 2014-2016 Ghibli and Quattroporte vehicles because the driver-side floor mat anchor may break, allowing the mat to trap the accelerator pedal.
Daimler Trucks North America is recalling 2014-2016 Freightliner Custom Chassis XCP vehicles because power steering hoses may fail due to high fluid temperatures, increasing crash risk.
United Pet Group is recalling Top Fin power filters for aquariums because a conductor can expose consumers to electric shock. No injuries have been reported.
American Grease Stick Company is recalling Carquest DOT5 Silicone Brake Fluid bottles manufactured between October 2013 and September 2015 due to missing or unclear labeling required by federal safety standards.
Ambient Weather is recalling about 57,000 radios that can overheat when plugged into AC power, posing a fire hazard.
Jayco is recalling 2016 Eagle fifth wheels and travel trailers because an unprotected solar battery cable may short circuit and cause a fire.
Hyundai is recalling 2011-2013 Equus and 2012 Genesis vehicles because a degrading wiper motor seal can cause corrosion and loss of wiper function, increasing crash risk in bad weather.
Terex is recalling 2008-2015 aerial devices because cylinder components may contact structural parts, potentially causing platform tilting and occupant falls.