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.
Toyota and GM are recalling specific Corolla, Corolla Matrix, and Pontiac Vibe vehicles because the front passenger air bag may not inflate properly in high temperatures.
Green Water, LLC is recalling several herbal tinctures and teas due to potential Salmonella contamination. The products were distributed nationwide.
Green Water, LLC is recalling several herbal tinctures and teas due to potential Salmonella contamination. The products were distributed nationwide.
Keto Farms LLC is recalling its Raspberry Gouda Fruit & Cheese Mix because an inspection found that coconut, a declared allergen, was missing from the label.
Becton Dickinson is recalling specific blood collection tubes because they can cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Siemens is recalling ACUSON NX2 ultrasound systems because internal testing found transducers may exceed defined acoustic output power values.
Becton Dickinson is recalling specific blood collection tubes because they may cause falsely elevated carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Keto Farms LLC is recalling specific varieties of Keto Snack Mix because the label failed to declare coconut, a major allergen. The recall covers 2,762 units distributed in the US, Canada, and several other countries.
Becton Dickinson is recalling BD Vacutainer Lithium Heparin blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Becton Dickinson is recalling BD Vacutainer PST Blood Collection Tubes because they may cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Siemens is recalling 17 MAGNETOM Prisma MRI devices due to a potential open port in the quench venting system when using the optional horizontal outlet.
Becton Dickinson is recalling BD Vacutainer Lithium Heparin blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with specific instruments.
Siemens is recalling 1,384 ACUSON NX3 diagnostic ultrasound systems worldwide because internal testing found transducers may exceed defined acoustic output power values.
Thoratec Corp. is recalling HeartMate 3 LVAS Implant Kits because an insufficiently seated C-Ring can cause the outflow graft to leak during implantation, rendering the device nonfunctional.
Siemens Medical Solutions is recalling two MAGNETOM Spectra MRI devices due to a potential open port in the quench venting system.
Radiometer America Inc is recalling ABL90 FLEX Analyzers due to software security vulnerabilities that may cause device shutdowns or reboots, potentially delaying medical treatment.
Becton Dickinson is recalling BD Vacutainer PST Gel and Lithium Heparin blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Becton Dickinson is recalling BD Vacutainer Lithium Heparin blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with specific instruments.
Green Water, LLC is recalling several herbal tinctures and teas due to potential Salmonella contamination. The products were distributed nationwide.
First Start Holdings is recalling Nosh Organic Fruit & Protein Soft Oat Bars due to potential mold contamination. The product was distributed nationwide through three US distributors and the company's website.
Medtech Products is recalling Clear Eyes Redness Relief eye drops due to concerns about quality assurance controls in the manufacturing facility.
Pro-Dex Inc is recalling sterile surgical driver battery packs due to visual particulates found within the Tyvek pouches.
Medtech Products, Inc. is recalling Clear Eyes Redness Relief eye drops due to concerns about quality assurance controls in the manufacturing facility.
Siemens Medical Solutions USA is recalling 143 MAGNETOM Aera MRI devices due to a potential open port in the quench venting system when using the optional horizontal outlet.
Medtech Products is recalling Clear Eyes Redness Relief eye drops due to concerns about quality assurance controls in the manufacturing facility.