---
title: "Remington MEDICAL, Automatic Cutting Needle, 18ga (1.3mm) x 20cm, REF NAC-182... — FDA record Z-0771-2023 | Is It on Recall"
description: "The stylet is longer than specified on the label"
url: https://isitonrecall.com/recall/fda-device-z-0771-2023-remington-medical-automatic-cutting-needle-18ga-1-3mm-x-20cm-ref-nac-1820m-1/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Remington MEDICAL, Automatic Cutting Needle, 18ga (1.3mm) x 20cm, REF NAC-1820M (1) — FDA record Z-0771-2023

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Dec 2, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Remington MEDICAL, Automatic Cutting Needle, 18ga (1.3mm) x 20cm, REF NAC-1820M (1)
- **Reason**: The stylet is longer than specified on the label
- **Classification**: Class II
- **Recalling firm**: Remington Medical, Inc.
- **Quantity**: 290 devices
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0771-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0771-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI/DI 00813079020936, Lot Number 2224920, exp. 2025-09/06 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

NC, WV, CA, PA, AL, TX

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Alabama](https://isitonrecall.com/state/alabama/)
- [California](https://isitonrecall.com/state/california/)
- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Texas](https://isitonrecall.com/state/texas/)
- [West Virginia](https://isitonrecall.com/state/west-virginia/)

## Dates in the source

- **Report date**: Jan 4, 2023
- **Recall initiation date**: Dec 2, 2022
- **Center classification date**: Dec 28, 2022
- **Termination date**: Mar 16, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0771-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Remington Medical, Inc. records](https://isitonrecall.com/brand/remington-medical-inc/)