---
title: "Allopurinol Tablets, USP 300mg, 100 Tablets per bottle, Rx only, Manufactured... — FDA record D-0583-2024 | Is It on Recall"
description: "Presence of foreign substance."
url: https://isitonrecall.com/recall/fda-drug-d-0583-2024-allopurinol-tablets-usp-300mg-100-tablets-per-bottle-rx-only-manufactured-by-dr-reddy-s-laboratories/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA drug enforcement

# Allopurinol Tablets, USP 300mg, 100 Tablets per bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories LA LLC, Sh... — FDA record D-0583-2024

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jun 7, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Allopurinol Tablets, USP 300mg, 100 Tablets per bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106 USA, NDC 55111-730-01.
- **Reason**: Presence of foreign substance.
- **Classification**: Class II
- **Recalling firm**: Dr. Reddy's Laboratories, Inc.
- **Quantity**: 20,520 units
- **Agency-reported status**: Terminated
- **Source record identifier**: D-0583-2024

[Open the official record](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0583-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | L2300594 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

IL, MS, OH

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Illinois](https://isitonrecall.com/state/illinois/)
- [Mississippi](https://isitonrecall.com/state/mississippi/)
- [Ohio](https://isitonrecall.com/state/ohio/)

## Dates in the source

- **Report date**: Jul 10, 2024
- **Recall initiation date**: Jun 7, 2024
- **Center classification date**: Jul 3, 2024
- **Termination date**: Dec 22, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0583-2024%22)

## Before changing a medicine

Follow urgent instructions in the current official recall notice. Speak to your pharmacist or prescriber before stopping or changing a prescribed medicine.

Talk to your doctor or pharmacist if you have questions or concerns about your medicine. [FDA medication recall guidance](https://www.fda.gov/drugs/drug-recalls/understanding-drug-recalls-what-know-and-what-do)

## Related records

[Medications records](https://isitonrecall.com/category/medications/) [Dr. Reddy's Laboratories, Inc. records](https://isitonrecall.com/brand/dr-reddy-s-laboratories-inc/)