# FDA recall D-1352-2022

> **Akron Pharma, Inc.** · Class III · drug recall initiated 2022-08-04.

## Product

Acetaminophen 325 mg tablets,  packaged in a) 100-count bottle (NDC 71399-8024-01); b) 1000-count bottle (NDC 71399-8024-02), Akorn Pharma Manufactured for: Akorn Pharma, Inc., Fairfield, NJ

## Reason for recall

Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.

## Distribution

Product was distributed to 6 distributors/wholesalers who may have further distributed the product.

## Key facts

- **Recall number:** D-1352-2022
- **Recalling firm:** Akron Pharma, Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-08-04
- **Report date:** 2022-08-24
- **Termination date:** 2023-12-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Fairfield, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1352-2022

## Citation

> AI Analytics. FDA recall D-1352-2022. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/D-1352-2022. Source: US FDA. Licensed CC0.

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