---
title: "EasyPoint Needle, 25G x 5/8\", REF: 82091 — FDA record Z-1293-2024 | Is It on Recall"
description: "The needle cannula of a retractable needle may detach from the needle holder in the patient."
url: https://isitonrecall.com/recall/fda-device-z-1293-2024-easypoint-needle-25g-x-5-8-ref-82091/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# EasyPoint Needle, 25G x 5/8", REF: 82091 — FDA record Z-1293-2024

Reported ongoing

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 Feb 5, 2024. 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**: EasyPoint Needle, 25G x 5/8", REF: 82091
- **Reason**: The needle cannula of a retractable needle may detach from the needle holder in the patient.
- **Classification**: Class II
- **Recalling firm**: Retractable Technologies, Inc.
- **Quantity**: 477,600
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1293-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1293-2024%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: 00613703820907. Lot: K220402. Expiration: 03/28/2027 |

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

## Distribution

US Nationwide distribution including in the states of NY, FL, IL, MA, UT, NJ, AZ, MO, WA, NC, CA, TX, NV, IN, PA, VA, IA, GA, TN, MI, OH, OK, CO, OR, SC, MN, CT.

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

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## Dates in the source

- **Report date**: Mar 20, 2024
- **Recall initiation date**: Feb 5, 2024
- **Center classification date**: Mar 14, 2024

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-1293-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Retractable Technologies, Inc. records](https://isitonrecall.com/brand/retractable-technologies-inc/)