---
title: "MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number... — FDA record Z-2654-2026 | Is It on Recall"
description: "Due to engineering sample labeled \"Not for Human Use\" being inadvertently shipped it the U.S. market."
url: https://isitonrecall.com/recall/fda-device-z-2654-2026-medline-111-gravity-set-w-3-needle-free-y-sites-ref-dyndtn0555-catalog-number-sam2461-udi-code-n-a-e/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number: SAM2461 UDI code: N/A Engineering Samp... — FDA record Z-2654-2026

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 4, 2026. 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**: MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number: SAM2461 UDI code: N/A Engineering Sample/Not for Human Use
- **Reason**: Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S. market.
- **Classification**: Class II
- **Recalling firm**: BD SWITZERLAND SARL
- **Quantity**: 50 devices
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2654-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2654-2026%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: SAM2461 REF: DYNDTN0555 UDI code: N/A Lot Number: 25X445 |

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

## Distribution

U.S.: IL O.U.S: N/A

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

- [Illinois](https://isitonrecall.com/state/illinois/)

## Dates in the source

- **Report date**: Jul 8, 2026
- **Recall initiation date**: Jun 4, 2026
- **Center classification date**: Jul 2, 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-2654-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [BD SWITZERLAND SARL records](https://isitonrecall.com/brand/bd-switzerland-sarl/)