State
72,940 recalls have nationwide distribution and so reach California. 13,245 additional recalls listed California specifically in their distribution scope.
Of the 13,245 recalls naming California we have scored against our rubric, 1,605 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,843 (21%) are Severe.
Which agencies issued them
These figures cover only the 13,245 recalls whose distribution notice names California 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 1 unit of the Evolution Upgrade 3.0T MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Philips North America is recalling 31 units of the Ingenia Elition X MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Aju Pharm is recalling 1,163 units of the Genesis Knotless Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
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 3 units of the SmartPath to dStream for XR and 3.0T because exported MR Elastography stiffness maps may show stiffness value errors.
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.
Gold Star Distribution is recalling toothbrushes and toothpaste-with-brush packs over potential exposure of rodents and rodent activity in its distribution center.
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.
Siemens is recalling 7 units of the LUMINOS Q.namix T fluoroscopic X-ray system because ortho images may not be flipped as preset and an image of a previous patient may be processed.
Philips North America is recalling 9 units of the MR 7700 MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Aju Pharm is recalling 233 units of the Fixone Hybrid Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Philips North America is recalling 5 units of the Ingenia Elition S because exported MR Elastography stiffness maps may show stiffness value errors.
Prima Vera Nueva is recalling 9,656 packages (4 tamales per package) of Roasted Pumpkin & White Cheddar Tamales over potential contamination with Listeria monocytogenes.
Daimler Coaches is recalling 2026 Mercedes-Benz Tourrider buses because a faulty door valve may prevent doors from opening, delaying emergency evacuation.
Bharat Bazar is recalling 180 packages of Soma Kitchen Natural Asafoetida over undeclared wheat.
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.
Prima Vera Nueva is recalling 30,327 packages (4 tamales per package) of Butternut Squash Tamales With Roasted Green Chiles over potential contamination with Listeria monocytogenes.
Keurig Dr Pepper is recalling 960 cartons of McCafe Premium Roast Decaf Coffee K-Cup Pods because the product is labeled as decaf but might contain caffeine.
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.
Medline is recalling 236 units 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.
Cerapedics is recalling 237 units of PearMatrix P-15 Peptide Enhanced Bone Graft, 1.0cc, over an incorrect expiration date.
Medline is recalling 857 units of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.
Ember is recalling certain 2026 E-Series and Overland Series travel trailers because the Federal Certification Label may list incorrect unloaded vehicle weight and cargo carrying capacity information.
Canon Medical Systems is recalling 98 units of the Alphenix INFX-8000F because fixing screws of the ceiling movement gear in the ceiling suspended arm may become loose.