# FDA recall Z-1925-2019

> **Madison Polymeric Engineering** · Class II · device recall initiated 2019-05-08.

## Product

First Step Draco Pad, Product Number EP-4D

## Reason for recall

This product has been contaminated with Stenotrophomonas lactiubi.

## Distribution

The products were distributed to the following US states:  AZ, CA, FL, IA, IL, IN, MA, MD, MO, PA, TN, TX, WA.

## Key facts

- **Recall number:** Z-1925-2019
- **Recalling firm:** Madison Polymeric Engineering
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-05-08
- **Report date:** 2019-07-10
- **Termination date:** 2020-07-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Branford, CT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1925-2019

## Citation

> AI Analytics. FDA recall Z-1925-2019. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/Z-1925-2019. Source: US FDA. Licensed CC0.

---

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