State
73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Arrow International is recalling Radial Artery Catheterization Kits because unsealed packaging may compromise product sterility.
Arrow International Inc. is recalling 416,055 ARROW JACC IV catheters because unsealed packaging may have compromised product sterility.
Arrow International is recalling 416,055 Pressure Injectable Multi-Lumen Central Venous Catheterization Kits because unsealed packaging may compromise product sterility.
Arrow International is recalling specific lots of Percutaneous Sheath Introducer Kits because unsealed packaging may compromise product sterility.
NordicNeuroLab AS is recalling 16 licenses of nordicTumorEx 1.0 software because a DICOM header error may cause incorrect image orientation labeling.
GE Lighting is recalling LED tube lamps sold at Lowe's because the pins can become energized during installation, posing electric shock and electrocution hazards.
Ohio Hickory Harvest Brand Products Inc. is recalling Hickory Harvest Island Fruit Mix due to Listeria monocytogenes found in a product stored in the same bin.
Medline is recalling sterile needle counters because packaging seal creep may compromise sterility. The product is used to count surgical sharps.
Arrow International is recalling Sheath Adapters with Cath-Gard shields because unsealed packaging may compromise product sterility.
Vernier Software & Technology is recalling Circuit Board 2 units because overheating switches can cause burns. About 4,200 units were sold between 2015 and 2018.
Arrow International Inc. is recalling 416,055 PICC catheters because unsealed packaging may have compromised product sterility.
Arrow International is recalling 416,055 central venous catheterization kits because unsealed packaging may compromise product sterility.
Arrow International is recalling 416,055 Multi-Lumen Central Venous Catheterization Kits because unsealed packaging may compromise product sterility.
Arrow International Inc is recalling 416,055 Multi-Lumen Central Venous Catheterization Kits because unsealed packaging may compromise product sterility.
Arrow International is recalling 416,055 Percutaneous Sheath Introducer Kits because unsealed packaging may compromise sterility. The recall covers products distributed in the US and 34 other countries.
Arrow International Inc. is recalling 416,055 Multi-Lumen Central Venous Catheterization Kits because unsealed packaging may compromise product sterility.
Arrow International is recalling 416,055 catheter hemostasis valves because unsealed packaging may compromise product sterility.
Siemens is recalling 33 SOMATOM Go.Up CT scanners in the US due to a potential software issue that may require patient rescans.
Arrow International is recalling VPS TipTracker Stylet Accessories because unsealed packaging may compromise product sterility.
Arrow International is recalling 416,055 central venous catheterization kits because unsealed packaging may compromise product sterility.
Torax Medical is recalling LINX Reflux Management Systems because a bead component may separate from an adjacent wire link, potentially resulting in a discontinuous or open device.
Siemens Healthcare Diagnostics is recalling Lot J1 of the Syva EMIT 2000 Theophylline Assay because it may show increased imprecision when used with a Beckman AU Clinical Chemistry System.
Siemens Medical Solutions is recalling 4 SOMATOM go.Now CT scanners in the US due to a potential software issue that may require patient rescans.
Arrow International Inc is recalling Maximal Barrier Drapes because unsealed packaging may compromise product sterility. The recall affects 416,055 units distributed in the US and 34 other countries.
Arrow International is recalling 416,055 central venous catheterization kits because unsealed packaging may compromise product sterility.