Severity 4 of 5
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.
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.
Renaissance Food Group is recalling Diced Red Onion (10 oz units) distributed to Alabama, Georgia, and South Carolina due to positive test results for Listeria monocytogenes in finished product.
Renaissance Food Group is recalling Hatch Chile Guacamole Blender due to positive test results for Listeria monocytogenes. Products were distributed to Alabama, Georgia, and South Carolina.
Antigua Farmacista Hand Sanitizer Ocean Citron (473 mL bottles) is being recalled because the product was found to contain benzene. The affected lot was distributed in Florida and Washington only.
Kenover Marketing Corp. is recalling Mighty Sesame Organic Tahini over potential Salmonella contamination. Approximately 13,766 units were distributed to stores across 20 states.
Renaissance Food Group is recalling Tri-Pepper Blend (7 oz units) due to positive test results for Listeria monocytogenes. All products manufactured with the same components are included in the recall.
Renaissance Food Group is recalling 12 oz packages of Snacking Peppers due to positive test results for Listeria monocytogenes. All products manufactured with the same components are affected.
Fresenius Kabi is recalling the Ivenix Infusion System (IIS) LVP Software version 5.2.0 because the display screen may freeze and become unresponsive, stopping medication flow and requiring immediate clinician intervention.
Renaissance Food Group is recalling Spicy Guacamole Blender products because positive test results confirmed Listeria monocytogenes contamination in the finished product.
Philips Respironics is recalling the Therapy Mask 3100 NC/SP because the product lacks warnings about magnetic components that may affect patients with implantable devices or metallic splinters in the eyes.
Renaissance Food Group is recalling Fajita Mix due to positive test results for Listeria monocytogenes in the finished product. The recall affects products distributed in Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Large Mild Chunky Guacamole (13 oz) due to positive test results for Listeria monocytogenes in the finished product.
Renaissance Food Group is recalling Asparagus Saute' products due to positive test results for Listeria monocytogenes. The recalled products were distributed to Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Mild Guacamole Blender products due to positive test results for Listeria monocytogenes. The affected products were distributed in Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Vegetable Bowl products because testing found Listeria monocytogenes contamination. The products were distributed to Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Small Medium Hatch Chile Pico de Gallo (9 oz units) because positive tests detected Listeria monocytogenes in the finished product. All products made with the same components are included in the recall.
Renaissance Food Group is recalling Mango Habanero Blender (9 oz units) because positive test results detected Listeria monocytogenes in the finished product.
Renaissance Food Group is recalling 106 units of Seasoned Squash Onion & Dill due to detection of Listeria monocytogenes. Products were distributed to Alabama, Georgia, and South Carolina.
Philips Respironics Amara View Full-Face Mask lacks critical safety warnings about magnetic components for patients with implantable medical devices. The Class I recall affects 5.6 million units worldwide.
FCA US is recalling 2019-2020 Ram 4500 and 5500 Cab Chassis vehicles because rear brake hoses may rupture, causing loss of braking ability.
Newmar is recalling certain 2023 Dutch Star motorhomes because the brake pedal may contact the dash panel, causing unintended brake engagement. This can lead to brake failure and increase crash risk.
Volkswagen is recalling 2022 and 2023 Atlas and Cross Sport vehicles because engine connecting rod bearings may become damaged, causing engine failure and stalling. This increases crash and fire risk.
Shyft Group is recalling 451 2022 Utilimaster Walk-In vans because the transmission shifter cable may contact the exhaust manifold, posing fire and crash risks.
Harley-Davidson is recalling 2022 RH975 Nightster motorcycles because the handlebar may not have been welded properly and could break, increasing crash risk.
Hyundai is recalling certain 2021-2022 vehicles due to transmission oil pump malfunction that can cause complete loss of drive power, increasing crash risk.
Rivian is recalling 2022 R1T, R1S, and EDV vehicles due to front steering knuckle fasteners that may be improperly tightened. A loose fastener could separate, causing loss of vehicle control and crash risk.