# FDA recall Z-1674-2020

> **Beckman Coulter Inc.** · Class II · device recall initiated 2019-12-13.

## Product

Beckman Coulter MicroScan PROMPT Inoculation System-D, Catalog Number B1026-10D, UDI: 15099590659561 - Product Usage: The Prompt Inoculation System-D is used to standardize inocula for microdilution antimicrobial susceptibility test.

## Reason for recall

Due to customer reports it has been determined that  the inoculation system contains the incorrect prompt wands. Use of the incorrect wands could result in false -susceptible results,  false-resistant results, possible misidentifications, or possible out-of-range Quality Control results.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of AL, AZ, AR, CA, CO, CT, DE, FL, GA, IL, IN, IA, KS, KY, LA, MD, MI, MS, NE, NY, NC, ND, OH, OK, PA, SD, TN, TX, UT, WV, WI, WY and countries of Canada, China, Japan, Paraguay.

## Key facts

- **Recall number:** Z-1674-2020
- **Recalling firm:** Beckman Coulter Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-12-13
- **Report date:** 2020-04-15
- **Termination date:** 2021-04-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Brea, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1674-2020

## Citation

> AI Analytics. FDA recall Z-1674-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1674-2020. Source: US FDA. Licensed CC0.

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