State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Medline Industries is recalling Suture Removal Packs because the iodine content is below the label claim of 0.85%.
Medline Industries is recalling RAD NECK ENT TRAY packs because the Povidone-Iodine prep pads contain subpotent iodine levels below the label claim.
Medline Industries is recalling sterile staple remover kits because the iodine concentration is below the labeled claim.
Medline Industries is recalling 73 cases of Incision & Drainage Trays because the Povidone-Iodine prep pads contain less iodine than labeled.
Baxter Healthcare is recalling Nexterone (amiodarone HCl) Premixed Injection because polyethylene particulate matter was identified in the product packaging.
Medline Industries is recalling Suture Removal Trays because the iodine concentration in the prep pads is below the labeled claim.
Medline is recalling 1,100 cases of GHS Suture Removal Trays because the iodine concentration is below the label claim.
Medline Industries is recalling hip replacement kits containing Povidone-Iodine prep pads with iodine levels below the label claim of 0.85%.
Medline Industries is recalling lidded catheter care trays because the povidone-iodine prep pads contain less iodine than the label claims.
Medline is recalling sterile incision and drainage trays because the povidone-iodine prep pads contain less iodine than labeled.
Medline Industries is recalling Suture Removal Kits because the iodine concentration is below the labeled claim of 0.85%.
Medline Industries is recalling 51 cases of Concordia Nurse Bag Kits because the Povidone-Iodine prep pads contain less iodine than the label claims.
Medline Industries is recalling sterile Povidone-Iodine prep pads because the iodine content is below the labeled 0.85% claim.
Medline Industries is recalling 600 cases of Laceration Trays because the Povidone-Iodine prep pads contain less iodine than the label claims.
Medline Industries is recalling Suture Removal Trays because the Povidone-Iodine prep pads contain less iodine than labeled.
Medline Industries is recalling 231 cases of Trunk Kits because the Povidone-Iodine prep pads contain less iodine than labeled.
Medline Industries is recalling Suture Removal Kits because the iodine concentration is below the labeled claim of 0.85%.
Medline Industries is recalling Povidone-Iodine prep pads because the iodine content is below the labeled claim of 0.85%.
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a set screw and sleeve assembly may have shifted during rework, potentially preventing proper assembly.
Medline Industries is recalling Vaginal Delivery CDS Packs because the iodine content is below the label claim.
Medline Industries is recalling Suture Removal Trays because the iodine concentration is below the labeled claim.
Medline Industries is recalling DC Line Kits because the iodine concentration in the prep pads is below the labeled claim.
Medline Industries is recalling sterile staple remover trays containing subpotent povidone-iodine prep pads. The iodine concentration is below the labeled claim of 0.85%.
Medline Industries is recalling 9,000 cases of Suture Removal Trays because the iodine concentration in the prep pads is below the labeled claim.
Medline is recalling Central Line Dressing Change Tray Kits because the iodine concentration in the prep pads is below the label claim.