# FDA recall D-1062-2013

> **Core Pharma Llc** · Class II · drug recall initiated 2013-07-02.

## Product

Pyridostigmine Bromide Tablets 60 mg, USP Rx Only 100 Tablets, Manufactured and Distributed by: CorePharma, LLC Middlesex, NJ 08846 NDC 64720-128-10  NDC 64720-128-10

## Reason for recall

Failed Stability Specifications: Pyridostigmine Bromide tablets, is being recalled due to an out of specification test result during stablity testing.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1062-2013
- **Recalling firm:** Core Pharma Llc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-07-02
- **Report date:** 2013-10-02
- **Termination date:** 2014-08-25

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1062-2013

## Citation

> AI Analytics. FDA recall D-1062-2013. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-1062-2013. Source: US FDA. Licensed CC0.

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