Severity 5 of 5
Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.
Severity 5 (Critical) covers recalls where deaths or serious injuries have been reported, or where the agency itself classified the action as the highest severity (FDA Class I, NHTSA 'death/serious injury reported'). These are the recalls you should treat as urgent — stop using the product immediately and follow the agency's guidance. Common Severity-5 categories are pathogen-contaminated ready-to-eat foods (Listeria, E. coli O157, Salmonella), drug products with confirmed adverse-event reports, and vehicle defects with documented fatal crashes.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
Taylor Farms Pacific Inc. is recalling specific lots of Roma tomatoes due to potential Salmonella contamination. The affected product was distributed in California, Arizona, Nevada, and Washington.
Gel Spice Co. is recalling Fresh Finds ground black pepper due to potential Salmonella contamination. Consumers should stop using the product.
Expo Fresh L.L.C is recalling 10,072 boxes of Roma Tomatoes due to potential Salmonella contamination. The product was distributed nationwide.
Mars Chocolate North America is recalling Twix Unwrapped Bites due to undeclared peanuts and eggs. The recall covers 13,560 pouches distributed nationwide.
Unique Pharmaceutical, Ltd is recalling one lot of N-Acetyl Cysteine 20% vials because testing revealed the presence of Herbaspirillum huttiense bacteria.
Eugene Oregon, Inc. is recalling Black Ant capsules because FDA testing found undeclared sildenafil. The product was marketed without an approved NDA or ANDA.
Eugene Oregon, Inc. is recalling African Black Ant capsules because FDA laboratory analyses found undeclared sildenafil. The product was marketed without an approved NDA/ANDA.
Baxter Healthcare is recalling 50,530 bags of Dianeal Low Calcium peritoneal dialysis solution due to the presence of particulate matter found during manufacturing.
Eugene Oregon, Inc. is recalling MOJO RISEN because FDA testing found undeclared sildenafil and the product was marketed without an approved NDA or ANDA.
Boskovich Farms is recalling diced Roma tomatoes sold in 24-ounce bags because they may be contaminated with Salmonella.
TJ's Place is recalling 8 oz. Basil Pesto Pasta tubs because they may be contaminated with Listeria monocytogenes.
BoKU International is recalling 10 oz. Boku Super Food 3.0 because it may be contaminated with Salmonella. The product was sold online directly to customers.
Silva International is recalling dehydrated minced green onion due to reported Salmonella contamination. The product was distributed in Wisconsin.
BoKU International is recalling Boku Super Food 2.0 (28.2 oz) because it may be contaminated with Salmonella. The product was sold online directly to customers.
Garden-Fresh Foods, Inc. is recalling Garden Fresh Egg Salad due to potential Listeria monocytogenes contamination. The product was distributed in Illinois, Indiana, Michigan, and Wisconsin.
Oriya Organics is recalling its Superfood Protein Medley because the product may be contaminated with Salmonella. The product was sold in Texas, Louisiana, and online to consumers in five states.
BoKU International is recalling Boku Super Protein 3.0 because it may be contaminated with Salmonella. The product was sold online directly to customers.
Foster Farms is recalling approximately 39,747 pounds of frozen chicken breast strips due to possible Listeria monocytogenes contamination. The product was distributed to California, Texas, Utah, and Washington.
Brooks Tropicals, LLC is recalling avocados found positive for Salmonella. The affected product was distributed in Florida, Georgia, Illinois, New Jersey, and New York.
Bristol-Myers Squibb is recalling Coumadin for Injection vials because metallic-like and cellulose fiber particles were found in retained samples.
Dean Foods is recalling Lehigh Valley Dairy Farms Orange Juice from concentrate because it contains undeclared dairy. The product was distributed in several Mid-Atlantic states.
Nova Products, Inc. is voluntarily recalling African Black Ant capsules because FDA testing found undeclared sildenafil, an active ingredient in erectile dysfunction drugs.
Dean Foods is recalling Lehigh Valley Dairy Farms Orange Juice from Concentrate because it contains undeclared dairy. The product was distributed in several Mid-Atlantic states and Washington, DC.
Baxter Healthcare is recalling 390,560 bags of 0.9% Sodium Chloride Injection USP due to the presence of particulate matter, including fibers and plastics.
Dean Foods is recalling Swiss Premium 100% Pure Orange Juice from Concentrate in half-gallon and one-gallon plastic containers due to undeclared dairy ingredients.