---
title: "HAIOU Needle retractable safety syringe with needle-(1ml syringe with 25G x 1... — FDA record Z-1506-2022 | Is It on Recall"
description: "Complaints received in which needle and needle holder have detached from the syringe after injection as well as needle not retracting into the syringe as per in"
url: https://isitonrecall.com/recall/fda-device-z-1506-2022-haiou-needle-retractable-safety-syringe-with-needle-1ml-syringe-with-25g-x-1-inch-needle-200-pieces/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# HAIOU Needle retractable safety syringe with needle-(1ml syringe with 25G x 1-inch needle} 200 pieces/box. Intended U... — FDA record Z-1506-2022

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 Jun 10, 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**: HAIOU Needle retractable safety syringe with needle-(1ml syringe with 25G x 1-inch needle} 200 pieces/box. Intended Use: Disposable sterile needle retractable safety syringe. Catalog Number: NRSS1-25G25
- **Reason**: Complaints received in which needle and needle holder have detached from the syringe after injection as well as needle not retracting into the syringe as per intended use, resulting in an increased risk of needle stick injury to the end user
- **Classification**: Class II
- **Recalling firm**: Guangdong Haiou Medical Apparatus Co., Ltd
- **Quantity**: 4,050,000 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1506-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1506-2022%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 | Lot Number: 20IB0 Exp. Date: 2025/09/04 |

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

## Distribution

US Nationwide distribution in the state of CA.

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**: Aug 17, 2022
- **Recall initiation date**: Jun 10, 2022
- **Center classification date**: Aug 5, 2022

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-1506-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Guangdong Haiou Medical Apparatus Co., Ltd records](https://isitonrecall.com/brand/guangdong-haiou-medical-apparatus-co-ltd/)
