# FDA recall Z-0196-2020

> **Valeritas, Incorporated** · Class II · device recall initiated 2019-07-03.

## Product

DEMO No Needle Corrugated Carton 30 U/D, Part Number 2260-02

## Reason for recall

There is a potential for "No Needle Demo Units" to contain a needle.

## Distribution

Nationwide within U.S.

## Key facts

- **Recall number:** Z-0196-2020
- **Recalling firm:** Valeritas, Incorporated
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-07-03
- **Report date:** 2019-11-06
- **Termination date:** 2020-06-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Marlborough, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0196-2020

## Citation

> AI Analytics. FDA recall Z-0196-2020. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/Z-0196-2020. Source: US FDA. Licensed CC0.

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