# FDA recall Z-1730-2019

> **Microbiologics Inc** · Class II · device recall initiated 2019-04-09.

## Product

Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI: 70845357041226    Product Usage:  On April 9, 2019, Microbiologics sent ACTION REQUIRED: MEDICAL DEVICE CORRECTION emails to their direct US consignees requesting them to complete a MEDICAL DEVICE CORRECTION FORM indicating how much product they had on hand.

## Reason for recall

Product with incorrect shelf life.

## Distribution

Worldwide Distribution - US Nationwide AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, MA, MD, MI, MO,MS, MT, NC, ND, NJ, NY, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WV, and WY.  Australia, Chile, Germany, New Zealand, and United Kingdom.

## Key facts

- **Recall number:** Z-1730-2019
- **Recalling firm:** Microbiologics Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2019-04-09
- **Report date:** 2019-06-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Cloud, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1730-2019

## Citation

> AI Analytics. FDA recall Z-1730-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1730-2019. Source: US FDA. Licensed CC0.

---

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