State
72,940 recalls have nationwide distribution and so reach Montana. 3,567 additional recalls listed Montana specifically in their distribution scope.
Of the 3,567 recalls naming Montana we have scored against our rubric, 689 (19%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 783 (22%) are Severe.
Which agencies issued them
These figures cover only the 3,567 recalls whose distribution notice names Montana specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Philips North America is recalling 10 units of the Ingenia 1.5T MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Gold Star Distribution is recalling toothbrushes and toothpaste-with-brush packs over potential exposure of rodents and rodent activity in its distribution center.
NIPRO Technical Services is recalling 499 units of Conductivity Standard Solution because a defect in the solution can cause meters to report incorrect conductivity values for dialysate.
Philips North America is recalling 3 units of the SmartPath to dStream for XR and 3.0T because exported MR Elastography stiffness maps may show stiffness value errors.
LSL Healthcare is recalling 1,400 Central Line Dressing Kits because the BD ChloraPrep Triple Swabsticks inside exhibit an open seal on the applicator packaging.
Philips North America is recalling 5 units of the Ingenia Elition S because exported MR Elastography stiffness maps may show stiffness value errors.
Philips North America is recalling 24 units of the Ingenia 3.0T MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Aju Pharm is recalling 1,088 units of the Fixone Biocomposite Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Aju Pharm is recalling 416 units of the AlternatiV+ Screw-In Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Aju Pharm is recalling 200 units of the Genesis Push-In Suture Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Cardinal Health is updating the instructions for use on 1,169,726 chest drainage units to clarify that the intended patient population is adults 18 years and older.
Philips North America is recalling 3 units of the Evolution Upgrade 1.5T MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Gold Star Distribution is recalling pregnancy tests over potential exposure of rodents and rodent activity in its distribution center.
Philips North America is recalling 6 units of the Ingenia 3.0T CX MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Baxter Healthcare is recalling 125,496 bottles of Sterile Water for Irrigation, 250 mL, after plastic particles from the bottle rim were observed floating in the solution.
Philips North America is recalling 1 unit of the SmartPath to dStream for 3.0T because exported MR Elastography stiffness maps may show stiffness value errors.
Philips North America is recalling 21 units of the Ingenia Ambition X because exported MR Elastography stiffness maps may show stiffness value errors.
Greenstone is recalling 3,456 cartons of methylprednisolone tablets Dosepak, 4 mg, because the blister foil was applied in the wrong orientation, giving incorrect dosing information.
Siemens is recalling 41 units of the LUMINOS Q.namix R fluoroscopic X-ray system because ortho images may not be flipped as preset and an image of a previous patient may be processed.
Aju Pharm is recalling 400 units of the Genesis Dual Thread Screw-In Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Medline is recalling 96 units of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.
Canon Medical Systems is recalling 3 units of the Alphenix INFX-8000H because fixing screws of the ceiling movement gear in the ceiling suspended arm may become loose.
Medline is recalling 1,928 total of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.
Medline is recalling 1,928 total of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.
CareFusion is recalling 189 BD Alaris Pump Modules, model 8100, because modules flashed with a daylight saving time timestamp may lose connectivity to hospital networks.