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.
Let's Do Lunch, Inc. is recalling Integrated Food Service Italian Submarine Sandwiches due to potential Listeria monocytogenes contamination. The products were distributed nationwide.
Let's Do Lunch, Inc. is recalling Cafe Favorites Turkey Ham & Cheese Deli Flatz due to potential Listeria monocytogenes contamination. The product was distributed nationwide in the U.S.
Integra LifeSciences Corp. is recalling Universal Wire Fixation Bolts because the Slotted Post broke during use at the surgical site.
Invacare Corporation is recalling 1,011 Bariatric home care beds because the junction boxes may spark, posing a fire hazard in the presence of flammable materials.
BioMerieux is recalling NucliSENS easyMAG Magnetic Silica reagents due to customer complaints about amplification performance issues.
Invacare Corporation is recalling 3,050 Bariatric Bed Foot Sections because a junction box defect may cause sparks and fire.
REV is recalling 2010-2016 Road Rescue emergency vehicles due to power control modules that may cause short circuits, risking electrical damage, loss of headlights, or fire.
Let's Do Lunch, Inc. is recalling Cafe Favorites Italian Deli Flatz due to potential Listeria monocytogenes contamination. The product was distributed nationwide in the U.S.
Invacare is recalling 2,184 Bariatric Beds because a defect in the Junction Box may cause sparks, posing a fire hazard in the presence of flammable materials.
Invacare is recalling 2,702 Bariatric Beds because the junction box may spark, posing a fire risk in the presence of flammable materials.
Integra LifeSciences is recalling 111 units of External Fixation System Slotted Posts because they broke during use at the surgical site.
Edan Diagnostics is recalling 521 EtCO2 modules used in patient monitors because they may provide incorrect CO2 readings.
Merge Healthcare is recalling PACS software versions V6.0.2.0 MR2 and earlier because patient names in the interface do not match the displayed images.
CH Guenther & Sons, Inc. is recalling Williams Chipotle Chili Seasoning because it contains undeclared wheat, a major allergen not listed on the label.
Zimmer Biomet Spine, Inc. is voluntarily recalling Zyston Transform Instrument Cases and Implant Kits because the implant locking mechanism is not functioning as intended.
Teleflex Medical is recalling Servo Humidifier 163 units because cracks may occur at the ISO female connectors.
Philips Medical Systems is recalling 205 Ingenuity CT units due to software issues in versions 4.1.3, 4.1.4, and 4.1.5 that could affect equipment performance.
Hill-Rom is recalling Volker 2080, 2082, S 280, and S 282 series hospital beds because the side rail latch may fail, causing the rail to lower and the patient to fall.
Xenith is recalling specific football helmets because the shells can crack, posing a risk of head injuries. No injuries have been reported.
Stryker Howmedica Osteonics Corp. is recalling 241 Exeter Rasp Handles because they may malfunction during use.
Zimmer Biomet Spine is recalling five Zyston Transform Implant Kits because the locking mechanism is not functioning as intended.
Williams Chipotle Taco Seasoning is being recalled because it contains undeclared wheat, a major allergen not listed on the label.
Stryker is recalling S3 MedSurg Beds because CPU board failures can cause the backrest electronic controls to stop working.
Synthes (USA) Products LLC is recalling 41 units of 2.4mm Titanium Locking Screws because they can break between the head and shaft due to a thin wall design.
Ortho Clinical Diagnostics is recalling VITROS Estradiol Reagent Packs because the drug Fulvestrant causes falsely high test results in postmenopausal women.