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.
Cantrell Drug Company is recalling 352 syringes of Heparin Sodium 0.5 USP UNITS/mL because stability data does not support the expiration date.
Arrow International Inc. is recalling specific lots of central venous catheters because kits labeled for 20 cm catheters may contain 16 cm catheters.
Cantrell Drug Company is recalling 212 syringes of Midazolam HCl that may contain less than the labeled amount of active ingredient.
Ergoactives is recalling 278 HeaterBaum Foot & Ankle Heating Pads because they were marketed without a cleared 510(k).
Musculoskeletal Transplant Foundation is recalling 114 AFT Diverted Tubes because an unsealed Tyvek pouch could introduce contamination into the sterile field.
Allergan Sales, LLC is recalling Tazorac (tazarotene) Gel 0.05% sample packs due to failed content uniformity specifications.
Allergan is recalling Tazorac (tazarotene) Gel 0.05% because the product failed content uniformity specifications. The recall covers 17,802 units distributed nationwide and in Puerto Rico.
Lifeline First Aid LLC is recalling CPR rescue kits because the included CPR shield mask is cleared only for prescription use, not over-the-counter.
ZYTO Technologies is voluntarily recalling ZYTO Tower devices and software because their marketing claims exceeded the scope of their FDA 510(k) clearance.
Zarbee's Naturals is recalling specific lots of Baby Vitamin D liquid supplements because some units contain elevated aerobic plate counts and do not meet visual appearance standards.
Synthes (USA) Products LLC is recalling 6,255 Ti Button Plate units because their MR safety information does not meet current ASTM standards.
Medtronic Navigation is recalling 63 O-arm 02 surgical x-ray imaging systems nationwide due to gaps in electronic product labeling and Instructions for Use compliance.
ZYTO Technologies is voluntarily recalling ZYTO Tower and software programs because their claims exceeded the scope of their FDA 510(k) clearance.
Exactech is recalling 14 Novation femoral stems because they were labeled with an incorrect Global Trade Item Number (GTIN). The error identifies the devices as a different product.
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 29 because incorrect calibration mathematics may cause biased test results for total iron-binding capacity.
Exactech is recalling 8 units of Novation Press-Fit Splined Femoral Stems because they are labeled with an incorrect Global Trade Item Number (GTIN).
Bernhardt Furniture is recalling about 1,700 Marquesa dressers and nightstands because they can tip over if not anchored, posing a risk of death or injury.
Chrysler is recalling specific 2014-2016 vehicles because a transmission wire harness defect may cause the vehicle to unexpectedly shift to neutral, increasing crash risk.
Honda is recalling 2015-2016 CB300F and CBR300R motorcycles because an improperly machined crankshaft may cause the engine to stall, increasing crash risk.
Nissan is recalling 1,140 Infiniti M35 Hybrid vehicles because a system overheat may cause the engine to shut off while driving, increasing crash risk.
Simmons Prepared Foods is recalling approximately 5,850 pounds of frozen, heat-treated chicken fritters due to possible E. coli O121 contamination from recalled flour.
Heil is recalling 2014-2016 trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.
Polar Tank Trailer is recalling 2014-2016 tank trailers because improperly machined brake valves may delay spring brake application, increasing the risk of the trailer rolling away.
Bombardier is recalling Can-Am Spyder F3-T motorcycles because an accessory passenger seat may fail to activate the vehicle stability system, increasing crash risk.
Honda is recalling 2016 Civic 2-Door vehicles because a damaged circuit board may cause side marker lights to fail, reducing visibility.