---
title: "injeTAK Adjustable Tip Needles Needle Sheath diameter 6Fr with 35-50cm in len... — FDA record Z-1478-2023 | Is It on Recall"
description: "The packaging may be damaged, compromising the sterile barrier."
url: https://isitonrecall.com/recall/fda-device-z-1478-2023-injetak-adjustable-tip-needles-needle-sheath-diameter-6fr-with-35-50cm-in-length-stainless-stell-nee/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# injeTAK Adjustable Tip Needles Needle Sheath diameter 6Fr with 35-50cm in length Stainless-stell needle cannula is 25... — FDA record Z-1478-2023

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 7, 2023. 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**: injeTAK Adjustable Tip Needles Needle Sheath diameter 6Fr with 35-50cm in length Stainless-stell needle cannula is 25 gauge
- **Reason**: The packaging may be damaged, compromising the sterile barrier.
- **Classification**: Class II
- **Recalling firm**: Labories Medical Technologies
- **Quantity**: 415,480 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1478-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1478-2023%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 | Model DIS199, UDI-DI (GTIN): 00627825000017 Lots: D198592, D211823, D19C094, D211825, D197765, D215573, D19B105, D214446, D19C097, D213099, D19C742, D214448, D201666, D213385, D202622, D216690, D203779, D217602, D204597, D21A632, D198638, D21B406, D204100, D219650, D201620, D221275, D207081, D218636, D205443, D21C155, D205441, D221088, D205445, D222083, D207623, D223087, D20A091, D224083, D20C092, D224386, D208579, D225586, D20C094, D225589, D20A092, D227088, D20B085, D226108, D211094, D228087 Model DIS201, UDI-DI (GTIN): 00627825000024 Lots: D19B109, D214447, D199716, D211094, D19B106, D214449, D19C789, D215574, D19C788, D216689, D19C098, D219083, D19C743, D217081, D201667, D218089, D203778, D21B407, D202623, D21B081, D204598, D21A082, D205444, D221277, D205440, D21C156, D203783, D221089, D205442, D221276, D204101, D222084, D203780, D224084, D207624, D221087, D207082, D222082, D208580, D223088, D205446, D226109, D20B086, D224387, D20A093, D227089, D20C095, D228088, D20C093, D226107, D211824, D228197, D211095, D229088, D211826, D22A099, D213100, D22A719, D213386, D229086 |

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

## Distribution

Worldwide distribution.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: May 10, 2023
- **Recall initiation date**: Feb 7, 2023
- **Center classification date**: Apr 28, 2023

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-1478-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Labories Medical Technologies records](https://isitonrecall.com/brand/labories-medical-technologies/)