What is an FDA recall classification (Class I, II, III)?

Class I is the most serious — a reasonable probability of serious health harm or death. Class II may cause temporary or reversible harm. Class III is unlikely to cause adverse health effects.

How often is this recall list updated?

Recalls are pulled live from the official openFDA enforcement database and refresh every few hours. Source: U.S. Food & Drug Administration (FDA) — openFDA enforcement API.

What should I do if I have a recalled food or drug?

Stop using the product, follow the recall instructions from the firm, and contact the recalling company or your pharmacy. Report adverse events to the FDA's MedWatch or food-safety line.

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Safety · Official FDA Data

Recent Food & Drug Recalls

The latest food, drug, and medical-device recalls reported to the U.S. FDA — with severity class, the reason, and affected products. Live data, updated through the day.

Food recalls →Drugs recalls →Medical devices recalls →

Latest Food recalls

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Class I — most seriousWIMay 27, 2026
PS Seasoning & Spices, Inc.
Product: Ellsworth Sour Cream + Onion Seasoning, Part #: 180000113. Net Wt 25.00 lbs (11.3kg). PS Seasoning & Spices 216 W Pleasant St Iron Ridge WI 53035
Reason: Product was made with milk powder recalled by the supplier due to Salmonella contamination.
FDA recall #H-0814-2026 · Ongoing
Class I — most seriousILMay 27, 2026
JOHN B SANFILIPPO & SONS INC
Product: Good & Gather Mexican Street Corn Trail Mix 8 oz bag UPC 085239270240, 8 bags per case
Reason: potential presence of Salmonella
FDA recall #H-0835-2026 · Ongoing
Class I — most seriousCAMay 27, 2026
Ghirardelli Chocolate Company
Product: GHIRARDELLI SWEET GROUND POWDER WHITE CHOCOLATE FLAVORED NET WT 50oz (3lbs 2oz) 1.41kg Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 747599620386

Latest Drugs recalls

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Class II — moderateOHMay 27, 2026
Safecor Health, LLC
Product: Atomoxetine Capsules HCL, 10 mg Capsules in unit dose foil strip, strips are packed in cartons of 100, Rx Only, Pkg by: Safecor, Columbus, OH 43204. NDC: 64380-474-01
Reason: Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule.
FDA recall #D-0538-2026 · Ongoing
Class II — moderateMNMay 27, 2026
IntegraDose Compounding Services LLC
Product: fentaNYL Citrate, Sterile CADD for Injection, 2,2500 mcg/50mL in Sterile Water, IntegraDose Compounding Services LLC, 3650 Victorie St N, Suite 900, Shoreview, MN, NDC 71139-6030-1.
Reason: Subpotent Drug
FDA recall #D-0548-2026 · Ongoing
Class II — moderateNJMay 27, 2026

Latest Medical devices recalls

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Class II — moderateCAMay 27, 2026
Becton, Dickinson and Company
Product: Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P
Reason: Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
FDA recall #Z-2203-2026 · Ongoing
Class II — moderateMay 27, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Product: Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (722064), Azurion 7 B12 (722067), Azurion 7 B20 (722068), Azurion 7 M12 (722078), Azurion 7 M20 (722079, 722224).
Reason: The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by restarting the system.
FDA recall #Z-2227-2026 · Ongoing
Class II — moderate

Frequently Asked Questions

What is an FDA recall classification (Class I, II, III)?: Class I is the most serious — a reasonable probability of serious health harm or death. Class II may cause temporary or reversible harm. Class III is unlikely to cause adverse health effects.
How often is this recall list updated?: Recalls are pulled live from the official openFDA enforcement database and refresh every few hours. Source: U.S. Food & Drug Administration (FDA) — openFDA enforcement API.
What should I do if I have a recalled food or drug?: Stop using the product, follow the recall instructions from the firm, and contact the recalling company or your pharmacy. Report adverse events to the FDA's MedWatch or food-safety line.

Data source: U.S. Food & Drug Administration (FDA) — openFDA enforcement API. Also see our vehicle recall check and consumer product recalls. Our methodology.