Health & Personal Care
HIGH
FDA DRUG
Fresenius Kabi Saline Solution Recalled for Lack of Sterility Assurance (2026)
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
immediate action Recalls
2,756 recalls tagged with “immediate action”.
Health & Personal Care
HIGH
FDA DRUG
BD and Fresenius Kabi Sodium Chloride Injection Recalled for Lack of Sterility Assurance (2026)
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
Health & Personal Care
HIGH
FDA DRUG
Fresenius Kabi 5% Dextrose Injection Recall Active Over Sterility Assurance Issue (2026)
Lack of Assurance of Sterility
DEXTROSE
Lack of
Health & Personal Care
HIGH
FDA DRUG
Fresenius Kabi 5% Dextrose Injection Recalled for Lack of Sterility Assurance (2026)
Lack of Assurance of Sterility
DEXTROSE
Lack of
Food & Beverages
HIGH
FDA FOOD
Nuts.com Espresso Malted Milk Balls Recalled for Undeclared Wheat and Soy (2026)
Undeclared Allergen - Wheat and Soy (from Soy Lecithin). The ingredient statement and allergen information do not include wheat or soy.
Nuts.com
Undeclared Allergen
Health & Personal Care
HIGH
FDA DEVICE
Siemens ARTIS pheno and ARTIS Icono Imaging Systems Recalled for Dose-Display Anomaly (2026)
Siemens Medical Solutions USA
During patient
Food & Beverages
HIGH
FDA FOOD
South Florida Food Pan de Bono Cheese Bread Recalled for Undeclared Soy in Florida (1,500 Units) 202
South Florida Food
Undeclared Soy.
Health & Personal Care
HIGH
FDA DRUG
Zydus Icosapent Ethyl Capsules Recalled for Oxidized Ingredient in 60,541 Bottles (2026)
Failed Tablet/Capsule specifications: Red dots inside capsule and melted capsule caused by oxidized Icosapent ethyl, the active ingredient.
ICOSAPENT ETHYL
Failed Tablet/Capsule
Food & Beverages
HIGH
FDA FOOD
Distribuidora de Alimentos Sendero Recalls 500 Doraditas de Azucar for Allergen Labeling (2026)
Distribuidora de Alimentos Sendero LLC recalled 500 Doraditas de Azucar sold in Texas. The products are missing Wheat and Soy allergen labeling on the package. Consumers should not eat them and should contact Sendero LLC for refund or replacement.
Distribuidora de Alimentos Sendero
Gorditas and
Food & Beverages
HIGH
FDA FOOD
Distribuidora de Alimentos Sendero Recalls 2,500 Gorditas de Azucar UPC 860010238134 (2026)
Distribuidora de Alimentos Sendero LLC recalls 2,500 Gorditas de Azucar and Doraditas distributed in Texas. The recall is due to missing Wheat and Soy allergens on the label. Consumers should stop using it and contact Sendero LLC for refund or replacement.
Distribuidora de Alimentos Sendero
Gorditas and
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray Recalled Over Expired-Lot
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Food & Beverages
HIGH
FDA FOOD
JFE FRANCHISING INC Dumpling Vegetable and Loaded Dumpling Vegetable Recalled for Glass (2 SKUs, 202
JFE FRANCHISING
Foreign Object
Health & Personal Care
HIGH
FDA DEVICE
Philips Vue Motion V12 Recall for 3,552 Units Over Cine Frame Sequencing Error (2026)
Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.
Philips Medical Systems Nederland B.V.
Potential that
Food & Beverages
HIGH
FDA FOOD
JFE Franchising Dumpling Party Tray Recall for Glass Contamination (2026)
JFE Franchising
Foreign Object
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Wayne Pneumothorax Set Recalled for Expired Shelf Life Labels
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Vehicles & Parts
HIGH
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Spectrum Central Venous Catheter Sets Recalled for Expired Shelf-Life Labels (2026)
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical CTO-6 Micro Wire Guide Recalled Worldwide Over Expired Shelf Life Labels (2026)
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Thal-Quick Chest Tube Tray Recalled for Expiration Dates Exceeding Shelf Life
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Tornier Tornier HRS Max Parts Recalled for Mislabeling, Incompatibility (2026)
Affected products were incorrectly labeled as Tornier HRS Max products. These parts are compatible with the Tornier HRS system only, and are incompatible with the Tornier HRS Max system.
Tornier
Affected products