State
72,940 recalls have nationwide distribution and so reach Maryland. 8,218 additional recalls listed Maryland specifically in their distribution scope.
Of the 8,218 recalls naming Maryland we have scored against our rubric, 996 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,131 (26%) are Severe.
Which agencies issued them
These figures cover only the 8,218 recalls whose distribution notice names Maryland specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Paragon 28 is recalling 20 Phantom Fibula Nails because out of specification thread depths may prevent the implant from mating with its mounting bolt, potentially requiring surgery to be aborted.
Philips North America is recalling the IntelliVue Patient Monitor MX750 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX600 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP60 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP80 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP70 over a potential issue where the monitors did not alarm.
Ventura Foods is recalling 700 cases of Publix Deli Carolina-Style Mustard BBQ Sauce after foreign objects, described as black plastic planting material, were found in granulated onion.
Blonde Beard's is recalling 4,888 8 oz bottles of Dojo Asian Wing Sauce because the product contains undeclared soy.
Philips North America is recalling the IntelliVue MP50 over a potential issue where the monitors did not alarm.
Prime Food Processing is recalling frozen Lava Bun with Green Tea Flavor because the products do not declare milk in the Contains statement or the ingredient statement.
Breckenridge Pharmaceutical is recalling 7,389 bottles of Duloxetine Delayed-Release Capsules, 60 mg, over the presence of N-nitroso-duloxetine above the FDA recommended limit.
Motor Coach Industries is recalling various transit bus models because the front door lower curb view glazing material is incorrect, which may reduce driver visibility and increase crash risk.
Breckenridge Pharmaceutical is recalling 3,397 bottles of Duloxetine Delayed-Release Capsules, 60 mg, over the presence of N-nitroso-duloxetine above the FDA recommended limit.
Philips North America is recalling the IntelliVue Patient Monitor MX800 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX500 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP5 over a potential issue where the monitors did not alarm.
Prime Food Processing is recalling 2,243 cases of frozen Lava Bun with Salted Egg Yolk because the products do not declare milk in the Contains statement or the ingredient statement.
Philips North America is recalling the IntelliVue Patient Monitor MX450 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX700 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP30 over a potential issue where the monitors did not alarm.
Accriva Diagnostics is recalling 20,250 Hemochron Activated Clotting Time Low-Range test cuvettes because a foreign object with sharp edges may pose a risk of injury if not detected before handling.
Philips North America is recalling the IntelliVue MP40 over a potential issue where the monitors did not alarm.
Hale inc is recalling 54 bottles of Lotsa Pasta Roasted Garlic Infused Olive Oil over the potential for Clostridium botulinum contamination.
Ventura Foods is recalling 3,556 cases of salad dressings sold under several brands after foreign objects, described as black plastic planting material, were found in granulated onion.
Philips North America is recalling the IntelliVue Patient Monitor MX550 over a potential issue where the monitors did not alarm.