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.
Newly Weds Foods is recalling B50829 breader due to potential Salmonella contamination. The FDA Class I recall affects approximately 6.5 million pounds distributed across 28 U.S. states and Canada.
Newly Weds Foods is recalling Crispy Breakfast Predust due to possible Salmonella contamination. Consumers should not eat affected products.
Newly Weds Foods recalls Karlin Chef Taco Seasoning (No MSG) in 50-pound bags due to potential Salmonella contamination. The product was distributed across 27 U.S. states and Canada.
Newly Weds Foods is recalling Roly Poly Chicken Seasoning due to potential Salmonella contamination. The 50-pound bags were distributed across multiple U.S. states and Canada.
Newly Weds Foods, Inc. is recalling Lees Noodle Mix following potential Salmonella contamination. The recall affects approximately 6.5 million pounds distributed across 28 US states and Canada.
Newly Weds Foods, Inc. is recalling B28336 Batter Mix in 50-pound bags due to potential Salmonella contamination. The product was distributed across the U.S. and Canada.
Newly Weds Foods, Inc. is recalling BREADER X1 breader product due to potential Salmonella contamination. The recall affects approximately 6.5 million pounds distributed across multiple US states and Canada.
Newly Weds Foods is recalling S19345 IQF Chicken Inject Seasoning due to potential Salmonella contamination. The product was distributed across 28 U.S. states and Canada.
Newly Weds Foods, Inc. is recalling batter mix products that may contain Salmonella. The affected products were distributed across 27 U.S. states and Canada.
Boreas Campers is recalling 2021-2022 XT travel trailers because a cooktop component may fracture and cause a gas leak, increasing fire risk.
Yamaha is recalling 2022 Tenere 700 motorcycles because front brake caliper bolts may have incorrect thread lengths, risking brake failure.
Ironman 4x4 is recalling Pro Forge upper control arms because the ball joint may fail, causing loss of steering control.
Daimler Trucks is recalling 2023-2024 Freightliner eCascadia vehicles because a defective e-axle weld may cause sudden loss of drive power, increasing crash risk.
VRURC portable chargers (model OD-B7) sold on Amazon.com from July 2021 through May 2023 can ignite and pose a fire hazard. One charger caught fire on a commercial flight, injuring four flight attendants.
The FDA is recalling approximately 302,652 Teleflex preformed oral endotracheal tubes nationwide due to reports of disconnection between the 15mm connector and the tube. Healthcare providers should immediately discontinue use of affected units.
TELEFLEX LLC is recalling Preformed AGT Oral Endotracheal Tubes because the 15mm connector may disconnect from the tube, creating a potential airway access risk.
Richin Trading Inc is recalling 141,192 units of Sun Wave Brand Jelly Cup due to a potential choking hazard. Affected products were distributed across 17 US states.
Teleflex LLC is recalling 19,842 preformed oral endotracheal tubes due to reports of 15mm connector disconnection. Affected devices were distributed nationwide.
TELEFLEX is recalling 1,570 units of Preformed AGT Oral Endotracheal Tubes nationwide due to reports of 15mm connector disconnection from the tubes. The disconnection could compromise airway management during patient ventilation.
Teleflex is recalling 244,120 Flexi-Set Cuffed Endotracheal Tubes due to reports that the 15mm connector may disconnect from the tube. Affected units were distributed nationwide.
TELEFLEX LLC is recalling 9,070 Preformed AGT Oral Endotracheal Tubes nationwide due to reports of 15mm connector disconnection. This medical device is used for airway management in hospital settings.
TELEFLEX is recalling 3,310 units of Slick Set Uncuffed Endotracheal Tubes (REF 170155) distributed nationwide due to reports of the 15mm connector disconnecting from the tube.
Teleflex recalls preformed AGT oral endotracheal tubes because the 15mm connector may disconnect from the tube, posing risk during patient use.
Teleflex is recalling Slick Set Uncuffed Endotracheal Tubes due to reports of the 15mm connector disconnecting from the tube. The recall affects 14,160 units distributed nationwide.
Teleflex is recalling 32,553 units of Flexi-Set Uncuffed Endotracheal Tubes nationwide due to reports of 15mm connector disconnections that could compromise airway management.