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 seriousHISeptember 2, 2026
H & U Inc. dba Sun Noodle
Product: Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base. Retail package net wt. 15.4oz. Product is ramen noodle kit which contains noodles and Soba soup packet. Item #05410 retail package, UPC 085315054108 Item #05410.1 cardboard box (12 packages per case), UPC 085315054105 Product is Perishable Frozen or Refrigerated and made by Sun Noodle Hawaii 1933 Colburn Street, Honolulu, HI
Reason: Soba sauce packet, which contains bonito, sardine, and mackerel (fish), was packed into Sura Tanmen Hot and Sour Flavor ramen noodle package kit, but fish species are not declared on finished product label.
FDA recall #H-1258-2026 · Terminated
Class I — most seriousCASeptember 2, 2026
KHONG GUAN (HQ)
Product: Glutinous Rice Balls with Black Sesame Filling NET WT. 14.1 OZ (400 g) Product of China UPC: 6908791000053
Reason: Undeclared peanuts.
FDA recall #H-1259-2026 · Ongoing
Class II — moderateCASeptember 2, 2026

Latest Drugs recalls

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Class II — moderateNCSeptember 2, 2026
ACCORD HEALTHCARE, INC.
Product: Levothyroxine Sodium Tablets, USP, 200 mcg (0.2 mg), packaged in a) 90-count bottles (NDC 16729-457-15) and b) 1000-count bottles (NDC 16729-457-17), Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India.
Reason: Subpotent Drug
FDA recall #D-0785-2026 · Ongoing
Class II — moderateOHSeptember 2, 2026
Hikma Pharmaceuticals USA INC.
Product: Ramipril Capsules USP, 10 mg, packaged in a) 100 Capsules (NDC 76282-673-01) and b) 500 Capsules (NDC 76282-673-05) bottles, Rx only, Manufactured for: Exelan Pharmaceuticals, Inc., Boca Raton, FL 33432, Manufactured by: West-Ward Columbus Inc., Columbus, OH 43228.
Reason: Failed Impurities/Degradation Specifications: OOS result obtained for a process impurity, dicyclohexylurea (DCU).
FDA recall #D-0831-2026 · Ongoing
Class II — moderate

Latest Medical devices recalls

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Class II — moderateILSeptember 2, 2026
Medline Industries, LP
Product: Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y; 2) NON MB MJR NEURO CRANI SM PK, Medline Kit SKU DYNJT6104; 3) CRANIOTOMY, Medline Kit SKU DYNJ903471I; 4) KIT CRANIOTOMY RFD, Medline Kit SKU DYNJ906496K.
Reason: Kits contain a potentially contaminated component which were recalled by the manufacturer
FDA recall #Z-3029-2026 · Ongoing
Class II — moderateILSeptember 2, 2026
Medline Industries, LP
Product: Medline convenience kits labeled as: 1) CMH LITHO MINOR PACK-LF, Medline Kit SKU DYNJ54362F; 2) EAST MAJOR LITHOTOMY, Medline Kit SKU DYNJ900957C; 3) GYN LAPAROTOMY, Medline Kit SKU DYNJ906804B; 4) UNIVERSAL GYN, Medline Kit SKU DYNJ910195A.
Reason: Kits contain a potentially contaminated component which were recalled by the manufacturer
FDA recall #Z-3028-2026 · 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.