Class II Recall — Risk of Temporary or Reversible Adverse Health Consequences

RIFAMPIN Rifampin Capsules USP 300mg, 30-count bottle, Rx Only, Manufactured for: Lupin Recall 2024

Official title: Rifampin Capsules USP 300mg, 30-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States, Manufactured Lupin Limited, Aurangabad 431 210 INDIA, NDC

MedicationsBy Recall Watch Editorial TeamJanuary 5, 2024Updated April 27, 2026

Verified source

U.S. Food and Drug Administration

This summary mirrors the official FDA notice issued January 5, 2024. Last synced from FDA: Apr 27, 2026.

Read official FDA notice

Rifampin Capsules USP 300mg, 30-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States, Manufactured Lupin Limited, Aurangabad 431 210 INDIA, NDC 68180-659-06

FDAClass II — Possible Riskdrug

What's recalled

Rifampin Capsules USP 300mg, 30-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States, Manufactured Lupin Limited, Aurangabad 431 210 INDIA, NDC 68180-659-06

Undeclared Allergen Alert

This recall involves undeclared allergens not listed on the label:

lupin

Affected Lot Numbers

Check your product label — do not use if your lot number appears below.

Lot Number
A200817 exp 1/2024

Why it was recalled

Subpotent Drug and Failed Impurities/Degradation Specifications

Where was it sold

Product was distributed to 32 Wholesale/distributor accounts who further distributed the product to 156 distribution sites.

nationwide

What to do

  1. Do not consume or use this product
  2. Check the lot numbers or UPC codes listed above
  3. Return the product to the store where you purchased it for a full refund
  4. Contact your healthcare provider if you have experienced any symptoms
View official FDA notice

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Frequently Asked Questions

Is the RIFAMPIN recall still active?

Yes, this recall is currently active as of January 5, 2024. Do not use or consume the affected product.

What lot numbers are affected?

Affected lot numbers: A200817 exp 1/2024. Check the label on your product.

What should I do if I have the recalled RIFAMPIN?

Do not consume or use this product. Return it to the store for a full refund, or dispose of it safely.

Why was RIFAMPIN recalled in 2024?

Subpotent Drug and Failed Impurities/Degradation Specifications