State
73,198 recalls have nationwide distribution and so reach California. 13,255 additional recalls listed California specifically in their distribution scope.
Of the 13,255 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 2,847 (21%) are Severe.
Which agencies issued them
These figures cover only the 13,255 recalls whose distribution notice names California specifically. The 73,198 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Reser's Fine Foods is recalling HEB Cilantro Cotija Dressing due to potential Listeria monocytogenes contamination. The dressing was distributed across multiple states in approximately 5,589 cases.
The FDA is recalling the HeartMate 3 Left Ventricular Assist System due to observed outflow graft deformation that can obstruct blood flow. Patients with implanted devices should contact their healthcare provider.
Reser's Fine Foods is recalling Cilantro Lime Crema products sold under Costco and Don Pancho labels due to Listeria monocytogenes contamination. Products were distributed across 16 states.
Dole Fresh Vegetables Inc is recalling Marketside Chopped Salad Kit Bacon Crunch due to potential Listeria monocytogenes contamination. Affected packages have lot codes B020-B036 with production dates from February 5, 2024 through February 21, 2024.
Cruiser RV is recalling 2023-2024 travel trailers and fifth wheels because a faulty LED circuit board in the cooktop may overheat and cause a fire.
ARROW International is recalling 1,160,470 QuickFlash radial artery catheterization devices due to a defective guidewire handle that can cause arterial vasospasm and vessel injury.
Fresh & Ready Foods LLC recalls Jack & Olive Ham Torta Sandwich due to Listeria monocytogenes contamination. The product was distributed in California, Nevada, Utah, and Arizona with use-by dates from January 27, 2024 to February 15, 2024.
Sprig & Sprout Ham Torta Sandwich is being recalled due to potential Listeria monocytogenes contamination. The product was distributed to CA, NV, UT, and AZ with Use By dates from January 27 to February 15, 2024.
Keystone RV Company is recalling various 2021-2024 RV models because the cooktop LED backlight circuit board may overheat and increase the risk of fire.
Dole Premium Kit Southwest Salad is being recalled due to potential Listeria monocytogenes contamination. Consumers who purchased affected products should not consume them.
Smiths Medical is recalling paraPAC plus 310 ventilators that may malfunction by delivering continuous gas flow instead of cycling breaths. The defect affects 10,140 units distributed worldwide and prevents proper ventilation.
Mack Trucks is recalling 2024-2025 LR natural gas vehicles because a missing fuse may render the methane detector inoperative, increasing the risk of fire or injury.
Reser's Fine Foods is recalling multiple chicken taco kits distributed across 16 states due to potential Listeria monocytogenes contamination in a repackaged cheese ingredient. Consumers should not consume affected products.
Nova Bus is recalling certain 2020-2024 LFS vehicles because the engine coolant return hose may fail, leading to engine shutdowns and increased crash risks.
Smiths Medical Pneupac Plus 300 ventilators may intermittently deliver continuous airflow instead of cycling breaths as designed. This malfunction affects 2,902 units distributed worldwide.
In2Bones, SAS is recalling I.B.S Compression screws due to a batch mix-up. Affected screws may have different lengths than indicated on their labels, creating a risk of improper surgical implantation.
Angiodynamics vascular guidewire introducers (600 units) may have internal defects preventing proper function during surgery. Defects could cause procedure delays and require device exchange.
Angiodynamics recalls MINI STICK MAX vascular guidewire introducers due to internal lumen defects that may prevent the guidewire from passing through during surgery, potentially requiring device exchange.
Novitium Pharma LLC recalls Digoxin 125mcg tablets nationwide due to cross contamination with mycophenolate mofetil, a different medication. Patients receiving contaminated tablets could experience unintended drug effects.
A Class II medical device recall has been issued for Directional Laser Probes due to potential difficulties extending, retracting, and directing the laser fiber tip. The issue affects 126 units distributed across multiple US states.
D.O.R.C. recalls 78 directional laser probes with Alcon/Lumenis connectors due to difficulties extending, retracting, or directing the laser fiber. The Class II recall affects units distributed across multiple U.S. states and Puerto Rico.
Beckman Coulter recalls Access Total T4 thyroxine assay due to imprecision that may cause erroneous or delayed diagnostic results.
Hikma Pharmaceuticals is recalling Infumorph 200 (morphine sulfate) ampuls because the sterile filter in the carton has an earlier expiration date than the medication, potentially compromising sterility.
Eugia US LLC is recalling Nicardipine Hydrochloride Injection nationwide due to failed impurity specifications. The 335,940 affected vials contain organic impurities exceeding acceptable standards.
Angiodynamics is recalling MINI STICK MAX guidewire introducers (155 units) due to manufacturing defects in the sheath hub that may prevent guidewire passage.