---
title: "Sterile Medline Convenience Kits: 1) MAJOR PACK L-F, Model Number: DYNJ038273... — FDA record Z-2592-2025 | Is It on Recall"
description: "Convenience kits labeled as sterile have not gone through the sterilization process."
url: https://isitonrecall.com/recall/fda-device-z-2592-2025-sterile-medline-convenience-kits-1-major-pack-l-f-model-number-dynj0382730o-2-lb-basic-custom-pack-m/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Sterile Medline Convenience Kits: 1) MAJOR PACK L-F, Model Number: DYNJ0382730O; 2) LB BASIC CUSTOM PACK, Model Numbe... — FDA record Z-2592-2025

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 Aug 8, 2025. 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**: Sterile Medline Convenience Kits: 1) MAJOR PACK L-F, Model Number: DYNJ0382730O; 2) LB BASIC CUSTOM PACK, Model Number: DYNJ61038B
- **Reason**: Convenience kits labeled as sterile have not gone through the sterilization process.
- **Classification**: Class I
- **Recalling firm**: Medline Industries, LP
- **Quantity**: 22 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2592-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2592-2025%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 | 1) DYNJ0382730O, UDI-DI: 10198459117992(each), 40198459117993(case), Lot Number: 25GBC583; 2) DYNJ61038B, UDI-DI: 10195327596316(each), 40195327596317(case), Lot Number: 25GBF720; |

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

## Distribution

US Distribution to States of: FL, MD, NJ, TN

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

- [Florida](https://isitonrecall.com/state/florida/)
- [Maryland](https://isitonrecall.com/state/maryland/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)

## Dates in the source

- **Report date**: Oct 8, 2025
- **Recall initiation date**: Aug 8, 2025
- **Center classification date**: Sep 26, 2025

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-2592-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medline Industries, LP records](https://isitonrecall.com/brand/medline-industries-lp/)