# FDA recall Z-0237-2019

> **Micro-Tech (Nanjing) Co., Ltd.** · Class II · device recall initiated 2018-09-20.

## Product

Single-Use Biopsy Forceps, JUMBO ALLIGATOR,3.2mm,  REF Catalog No. NBF13-01130230, UPN BF40180 (Pouch level) - BF40181(Case box level)  BF40182 (Carton box level) - BF40183(Over shipper level), STERILE

## Reason for recall

Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units

## Distribution

US Nationwide Distribution in the states of AL, CA, IN, FL, GA, MO, MT, NV, OK, OR, PA TX & Washington D.C.

## Key facts

- **Recall number:** Z-0237-2019
- **Recalling firm:** Micro-Tech (Nanjing) Co., Ltd.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-09-20
- **Report date:** 2018-10-31
- **Termination date:** 2019-10-21

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0237-2019

## Citation

> AI Analytics. FDA recall Z-0237-2019. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/Z-0237-2019. Source: US FDA. Licensed CC0.

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