# FDA recall D-0128-2018

> **L. Perrigo Company** · Class II · drug recall initiated 2017-11-08.

## Product

Maximum Strength Zephrex-D, Pseudoephedrine HCl, 30 mg, Nasal Decongestant.  24 softgel tablets per paper carton, Distributed by Perrigo, Allegan, MI 49010, NDC 70085-151-01

## Reason for recall

Microbial Contamination of Non-Sterile Products

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0128-2018
- **Recalling firm:** L. Perrigo Company
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-11-08
- **Report date:** 2017-12-27
- **Termination date:** 2018-12-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Allegan, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0128-2018

## Citation

> AI Analytics. FDA recall D-0128-2018. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/D-0128-2018. Source: US FDA. Licensed CC0.

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