# FDA recall Z-1877-2018

> **Micro-Tech (Nanjing) Co., Ltd.** · Class II · device recall initiated 2018-03-12.

## Product

Trident Endoscopic Ultrasonic Biopsy Needle (FNB)

## Reason for recall

The combination of the firmness of the mass, the potential endoscope and elevator position combined with the force required to penetrate the mass may contribute to the breakage of the needle in the human body, which could cause injury.

## Distribution

US distribution to one distributor in MI.

## Key facts

- **Recall number:** Z-1877-2018
- **Recalling firm:** Micro-Tech (Nanjing) Co., Ltd.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-03-12
- **Report date:** 2018-05-23
- **Termination date:** 2018-08-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Nanjing, China

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1877-2018

## Citation

> AI Analytics. FDA recall Z-1877-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-1877-2018. Source: US FDA. Licensed CC0.

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