Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
HandNatural is recalling H&Natural Tejocote Root dietary supplement because the product contains yellow oleander and its components, which pose a health risk.
SonarMed Inc is recalling 690 units of the AW-S030 NEO SONARMED SENSOR because the sensor fails to detect partial airway obstruction. The devices were distributed across 20 US states.
HandNatural is recalling H&Natural Brazil Seed 30-piece supplements due to the presence of yellow oleander and its components in the product. Consumers should stop using the product immediately and dispose of it safely.
BMW is recalling 2014-2015 2, 3, and 4 Series vehicles because head air bag inflators may fail, posing an injury risk.
Kia is recalling certain 2024 Sorento vehicles because the motor driven power steering wiring harness may be incorrectly assembled, which can result in a loss of power steering assist.
REV Ambulance Group Orlando is recalling 76 ambulances from 2019-2024 because a firmware defect may cause electrical circuits to overheat and increase the risk of fire.
Robeson Enterprises is recalling Mo' Money Pie due to undeclared soy allergen on the label. The product was distributed to Georgia, North Carolina, and South Carolina.
Robeson Enterprises is recalling Deep South Tomato Pie because the label does not list sub-ingredients, and pimento cheese in the product may contain undeclared eggs. Consumers with egg allergies should not consume this product.
Robeson Enterprises recalls PIES & SIDES brand pumpkin pie because the product label fails to list undeclared milk and eggs, posing a risk to consumers with these allergies.
Fresenius Kabi USA is recalling Ivenix Infusion System software version 5.8.0 for anomalies that could cause incorrect medication dosing or therapy delays. The Class I recall affects 17 units across 13 US states.
Eugia US LLC is recalling Methocarbamol Injection nationwide due to particulate matter contamination. The FDA classified this as a Class I recall affecting lot 3MC23011 (expiration 11/30/2026).
Spencer is recalling 2024 Pumper vehicles because a firmware defect in specific electrical nodes may cause overloaded circuits and increase the risk of fire.
Naturz Organics is recalling Organic Pea Protein (Item Code NO-OPP-80, 20 kg bags) due to possible salmonella contamination. The recall affects bulk product distributed to one consignee in Wisconsin.
Robeson Enterprises is recalling 482 units of PIES & SIDES Baked Mac and Cheese because the label fails to declare egg as an allergen and does not list any ingredients. Products were distributed to Georgia, North Carolina, and South Carolina.
Alipotec Raiz de Tejocote dietary supplements are being recalled because they contain toxic yellow oleander instead of tejocote. All 280 bottles were distributed nationwide.
Kawasaki is recalling 2024 Z900RS motorcycles because a manufacturing error may cause front tire blistering, increasing crash risk.
Forest River is recalling 2024 Cardinal and Wildcat fifth wheel trailers because the rear towing hitch may be used without locking the turning point, increasing crash risk.
Autocar is recalling 2022-2023 Legend dump trucks because a hoist mounting pin may fail, posing injury and crash risks.
Keystone RV is recalling 214 specific 2024 trailer models because the suspension equalizer may allow the axle to contact the frame, increasing crash risk.
Jugader Zipline Kits sold on Amazon.com from March 2020 through June 2023 are recalled because the stainless-steel cable can break, causing falls. The manufacturer has received 20 reports of cable breakage resulting in nine injuries.
Johnson Health Tech North America is expanding its recall of Matrix T1 and T3 Series commercial treadmills due to a fire hazard from loose power cords. About 9,700 additional units are affected.
Hi-Tech E.V.S. is recalling 2020-2023 Spartan Gladiator and Metrostar fire trucks because a firmware defect in specific nodes may cause electrical circuits to overheat and increase the risk of fire.
SleepNet is updating safety warnings and contraindications for its Mojo Non Vented Full Face Mask due to magnet content. All 11,874 affected units are subject to this warning update.
SleepNet is recalling the Phantom 2 Nasal Vented Mask to update contraindications and warning information related to magnets in the device. The recall affects 2,417 units distributed worldwide.
SleepNet Corporation is recalling 2,787 units of the Mojo 2 Full Face Vented Mask due to updates needed for contraindications and warning language regarding magnets in the device. Worldwide distribution.