# FDA recall Z-0771-2023

> **Remington Medical, Inc.** · Class II · device recall initiated 2022-12-02.

## Product

Remington MEDICAL, Automatic Cutting Needle, 18ga (1.3mm) x 20cm, REF NAC-1820M (1)

## Reason for recall

The stylet is longer than specified on the label

## Distribution

NC, WV, CA, PA, AL, TX

## Key facts

- **Recall number:** Z-0771-2023
- **Recalling firm:** Remington Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-12-02
- **Report date:** 2023-01-04
- **Termination date:** 2026-03-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Alpharetta, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0771-2023

## Citation

> AI Analytics. FDA recall Z-0771-2023. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0771-2023. Source: US FDA. Licensed CC0.

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