---
title: "Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706 — FDA record Z-0470-2025 | Is It on Recall"
description: "Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing pro"
url: https://isitonrecall.com/recall/fda-device-z-0470-2025-posi-stop-injection-needle-23-gauge-catalog-number-4706/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706 — FDA record Z-0470-2025

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 Oct 4, 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**: Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706
- **Reason**: Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
- **Classification**: Class II
- **Recalling firm**: Hobbs Medical, Inc.
- **Quantity**: 6 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0470-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0470-2025%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 | Catalog Number: 4706; UDI-DI: M84947060; Lot Number: SD09-23-089. |

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

## Distribution

Worldwide - US Nationwide distribution in the states of CT, GA, IN, MI, MN, MS, NH, NJ, NY, OH, TN, VT, WA, WI, WV and the country of Canada.

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

- [Alaska](https://isitonrecall.com/state/alaska/)
- [Alabama](https://isitonrecall.com/state/alabama/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Nov 27, 2024
- **Recall initiation date**: Oct 4, 2024
- **Center classification date**: Nov 15, 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-0470-2025%22)

## Related records

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