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
Philips has recalled 50 units of its GYROSCAN ACS-NT MRI systems. The patient support table floor plate may be incorrectly installed, potentially posing a safety risk.
Artivion is recalling one CryoValve SG cryopreserved heart valve contaminated with Staphylococcus aureus, detected during organ donation screening. No illnesses have been reported.
Philips is recalling 12 Intera 1.5T MRI systems worldwide because the patient support table floor plate may be incorrectly installed. Healthcare facilities should verify proper installation.
Philips Evolution 3.0T MRI systems may have an incorrectly installed patient support table floor plate, creating a potential safety risk. Affected facilities should verify proper installation.
Philips is recalling 344 Ingenia Ambition S MRI systems because the patient support table floor plate may be incorrectly installed.
Philips is recalling 9 Intera 3.0T Quasar Dual MRI systems (Model 781150) distributed worldwide. The patient support table floor plate may be incorrectly installed on these units.
Approximately 21,723 Masimo Rad-G pulse oximeters may randomly power off and on, causing temporary loss of patient monitoring. The FDA classified this as a Class II recall affecting devices distributed worldwide.
Full Speed Ahead is recalling Gossamer Pro AGX+ cranksets that can loosen or detach from bicycles, creating a fall hazard. The company has received 277 reports of loosening or detachment but no injuries to date.
Randder 2-Pack Liquid Fuel Bottles in 750mL and 1500mL sizes sold on Amazon are recalled because their closures do not meet child-resistant requirements under the Children's Gasoline Burn Prevention Act, posing a risk of burns and poisoning to children.
Gasaciods children's helmets sold on Temu.com fail to meet federal safety standards for bicycle helmets and do not adequately protect against head injury in a crash. Consumers should stop using them immediately.
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 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.
Alipotec Raiz de Tejocote dietary supplements are being recalled because they contain toxic yellow oleander instead of tejocote. All 280 bottles were distributed nationwide.
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).
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.
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.
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.
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.
Baxter Healthcare is recalling power cord models globally because the insulation does not meet electrical safety standards, creating a potential risk of electrical shock or fire.
PIES & SIDES Broccoli Casserole by Robeson Enterprises is recalled because the product label does not list ingredients. The product contains wheat, eggs, milk, soy, and fish.
Boston Scientific is recalling 572 EndoVive PEG feeding tube kits due to a blocked lumen in the barb connector that may prevent guidewire advancement during placement, potentially requiring device exchange and increasing risk of complications.
Baxter Healthcare is recalling Connex ProBP 3400 blood pressure monitors due to power cord insulation defects that fail to meet electrical safety standards. Approximately 11,154 units are affected globally.
Robeson Enterprises is recalling Pies & Sides Hashbrown Casserole because the label lacks an ingredient list, preventing consumers from identifying allergens. The product was distributed in Georgia, North Carolina, and South Carolina.
Boston Scientific is recalling the EndoVive 20Fr PEG feeding kit due to blockage in the barb connector that can prevent proper placement. The blockage may lead to prolonged procedures, bleeding, gastric leakage, and aspiration risk.
Intuitive Surgical recalled 53 da Vinci SP Surgical System Patient Carts due to inadequate welds in the instrument arm joints. These welds may cause tissue injuries, conversion to open surgery, or user pinching injuries.