# FDA recall Z-2656-2017

> **JAS Diagnostics Inc.** · Class II · device recall initiated 2017-04-21.

## Product

Drew Scientific DREW 3-PAC Reagent Kit containing: 5L Diluent, 750 mL Enzymatic Cleaner, and 125 mL Lysing Reagent.

## Reason for recall

May result in elevated platelet backgrounds during routine startup/background checks.

## Distribution

AL, AR, CA, FL, GA, IA, IN, LA, MA, MN, MO, NC, NE, NY, SC, TN, TX, and  Puerto Rico   United Arab Emirates, Bolivia, Republic of C¿te dIvoire, Colombia, Costa Rica, Ecuador, Egypt, Indonesia, Iraq, Italy, Korea, Mexico, Russia, Philippines, Slovenia, Tunisia, Venezuela, and Vietnam

## Key facts

- **Recall number:** Z-2656-2017
- **Recalling firm:** JAS Diagnostics Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-04-21
- **Report date:** 2017-07-12
- **Termination date:** 2020-01-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Miami Lakes, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2656-2017

## Citation

> AI Analytics. FDA recall Z-2656-2017. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-2656-2017. Source: US FDA. Licensed CC0.

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