State
73,738 recalls have nationwide distribution and so reach Oklahoma. 5,822 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,822 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 1,493 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,822 recalls whose distribution notice names Oklahoma specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Arrow International is recalling 159 units of Arrow PICC catheters because the expiration date printed on the packaging is incorrect.
Arrow International is recalling 991 units of Arrow PICC with Chloraguard Technology due to incorrect expiration dates on the product.
Arrow International Inc is recalling 185 units of Arrow PICC with Chloraguard Technology due to incorrect expiration dates on the packaging.
Arrow International Inc. is recalling 77 units of Arrowg+ard Blue Advance JACC products because they were labeled with an incorrect expiration date.
Arrow International Inc. is recalling Arrow PICC with Chloraguard Technology due to an incorrect expiration date on the product.
Arrow International Inc is recalling Arrowg+ard Blue Advance JACC products due to an incorrect expiration date. The recall involves 174 units distributed nationwide.
Sun Pharmaceutical is recalling Allergy Relief D tablets because testing showed impurities and degradation levels above or near specification limits.
Arrow International Inc. is recalling 135 units of Arrow PICC with Chloraguard Technology due to an incorrect expiration date.
Arrow International Inc is recalling 578 units of Arrow PICC with Chloraguard Technology due to an incorrect expiration date.
Cytocell Ltd. is recalling Aquarius D13S319 Plus Deletion Probes because the chromomap on the package insert contains an error.
Akorn Inc. is recalling 16,216 cartons of Myorisan isotretinoin capsules because secondary cartons incorrectly state 40 mg instead of 30 mg.
Arrow International Inc is recalling 16 units of Arrowg+ard Blue Advance JACC because the product has an incorrect expiration date.
Arrow International Inc. is recalling 12 units of JACC central catheters because the expiration date printed on the packaging is incorrect.
Arrow International Inc. is recalling 6 units of Arrow JACC Central Catheters because the expiration date is incorrect.
Teligent Pharma is recalling Betamethasone Dipropionate Ointment 0.05% due to failed impurities and degradation specifications.
Arrow International Inc. is recalling 3 units of Arrow JACC with Chloragard Technology due to an incorrect expiration date.
Charles Machine is recalling 2018-2019 Ditch Witch trailers because hitch lock nuts may fail to clamp the load, increasing crash risk.
Daimler Vans USA is recalling 2018-2019 Mercedes-Benz Metris vehicles because a steering sensor defect may cause the electric power steering assist to deactivate, increasing crash risk.
QTOP USA is recalling specific LED work light replacement bulbs because they can overheat and cause fires. Consumers should stop using the bulbs and contact the company for a refund.
West Marine is recalling about 11,600 folding deck chairs because a lock nut can loosen, posing fall and injury hazards. No injuries have been reported.
Mazda is recalling 2010-2011 RX-8 vehicles because the passenger air bag inflator may explode during deployment, potentially causing serious injury or death.
Oshkosh is recalling 2019 McNeilus Meridian, Atlantic, and Contender front loader trucks because battery cables may rub against the fuse box bracket, increasing the risk of fire.
Oshkosh is recalling 2018 McNeilus Bridgemaster V Concrete Mixers because an incorrect filler neck part may cause the tank to overpressurize and rupture.
Altec is recalling 2003-2019 aerial devices due to potential air brake pressure loss. Owners should contact dealers for free inspection and repair.
Spartan Motors is recalling 4,534 Utilimaster Walk-In Vans because a brake pedal clip may detach, causing brake light failure or pedal detachment.