# FDA recall Z-2001-2019

> **Terumo Medical Corporation** · Class II · device recall initiated 2019-02-08.

## Product

Terumo Sur-vet Needle, 25G x 5/8", Product Code 100220

## Reason for recall

There is a potential for a loss of package integrity that may compromise the sterility of the product.

## Distribution

The products were distributed to the following US states: FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, and TX.

## Key facts

- **Recall number:** Z-2001-2019
- **Recalling firm:** Terumo Medical Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-02-08
- **Report date:** 2019-07-31
- **Termination date:** 2020-05-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Elkton, MD, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2001-2019

## Citation

> AI Analytics. FDA recall Z-2001-2019. Retrieved 2026-06-01 from https://api.ai-analytics.org/recall/Z-2001-2019. Source: US FDA. Licensed CC0.

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