# FDA recall D-1128-2017

> **Mckesson Packaging Services** · Class III · drug recall initiated 2017-08-28.

## Product

Propafenone Hydrochloride tablets, 150 mg, packaged in 10 x 10 unit dose cards (100-count box), Rx only, Manufactured By: Watson Pharmaceuticals 311 Bonnie Circle Corona, CA 92880, NDC 63739-509-10

## Reason for recall

Failed moisture limits: Out of specification for moisture content.

## Distribution

PA, OH, IL, CO, LA

## Key facts

- **Recall number:** D-1128-2017
- **Recalling firm:** Mckesson Packaging Services
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-08-28
- **Report date:** 2017-09-13
- **Termination date:** 2020-05-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Concord, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1128-2017

## Citation

> AI Analytics. FDA recall D-1128-2017. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/D-1128-2017. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
