State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Hitachi Medical Systems America Inc is recalling 39 Scenaria Whole-body X-ray CT Systems because cables to the controller unit may not be affixed properly, creating a risk of detachment during scanning.
Zimmer Biomet is recalling cable buttons for NCB Polyaxial Locking Plates because non-highly polished implants may adhere to the packaging bag.
Ortho-Clinical Diagnostics is recalling VITROS K+ Slides because a mechanical failure may cause intermittent slide dispense issues.
Western / Scott Fetzer is recalling 143,164 Grab n Go Opti VIPR oxygen systems because the control knob may rotate beyond its functional range, limiting access to flow settings.
Zimmer Biomet is recalling 5.4 million tibial plates because non-highly polished implants may adhere to the packaging bag.
Ortho-Clinical Diagnostics is recalling VITROS chemistry Cl- Slides because the anti-backup platen may fail to advance, causing intermittent slide dispense issues.
Zimmer Biomet is recalling 5.4 million ceramic femoral heads because non-highly polished implants may adhere to the LDPE bag packaging.
Pega Medical Inc. is recalling 31 SCFE Knobs for Driver because screws may loosen during ultrasonic cleaning and fall out.
Zimmer Biomet is recalling ZPLP Fibular Plates because non-highly polished implants may adhere to the LDPE bag packaging.
Zimmer Biomet is recalling NCB Periprosthetic Proximal Femoral Plates because non-highly polished implants may adhere to the packaging bag.
Zimmer Biomet is recalling CLS Brevius Stem Kinectiv hip prostheses because non-highly polished implants may adhere to the packaging bag.
Randox Laboratories is recalling 17 Rheumatoid Factor Standard kits because assigned values over-recovered against reference material. The values have been adjusted to align with the reference standard.
Zimmer Biomet is recalling various fixation systems and accessories because non-highly polished implants may adhere to the LDPE bag.
Zimmer Biomet is recalling 5.4 million Universal Locking Plates because non-highly polished implants may adhere to the packaging bag.
Zimmer Biomet is recalling specific periarticular plates because non-highly polished implants may adhere to the packaging bag.
Zimmer Biomet is recalling 5,459,583 sterile distal lateral femoral locking plates because non-highly polished implants may adhere to the packaging bag.
Biomedical Polymers, Inc. is recalling 108,000 Hemo-Drop Blood Dispensers because the metal cannula may break or fail to pierce the specimen tube.
Zimmer Biomet is recalling specific wrist implants because non-highly polished devices may adhere to the packaging bag.
Zimmer Biomet is recalling Fitmore Hip Stems because non-highly polished implants may adhere to the LDPE bag used in previous packaging configurations.
Zimmer Biomet is recalling NCB Straight Narrow Plates because non-highly polished implants may adhere to the LDPE bag packaging.
Zimmer Biomet is recalling Prox Lat Tib Lock Plates and Dist Med Tib Lock Plates because non-highly polished implants may adhere to the LDPE bag packaging.
Zimmer Biomet is recalling 5,459,583 LPS-MOB Articular Surface Implants because non-highly polished implants may adhere to the LDPE bag.
Zimmer Biomet is recalling 5.4 million periarticular locking elbow plates because non-highly polished implants may adhere to the packaging bag.
Zimmer Biomet is recalling various surgical screws and reamers because non-highly polished implants may adhere to the LDPE bag.
Ortho-Clinical Diagnostics is recalling VITROS chemistry Cl- Slides because an anti-backup platen failure may cause intermittent slide dispense issues.