---
title: "Medline Convenience kits labeled as: 1) MINOR BASIC PACK-LF, Pack Number DYNJ... — FDA record Z-3025-2024 | Is It on Recall"
description: "Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have bee"
url: https://isitonrecall.com/recall/fda-device-z-3025-2024-medline-convenience-kits-labeled-as-1-minor-basic-pack-lf-pack-number-dynj0281516m-2-minor-acute-pac/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Medline Convenience kits labeled as: 1) MINOR BASIC PACK-LF, Pack Number DYNJ0281516M; 2) MINOR ACUTE PACK-LF, Pack N... — FDA record Z-3025-2024

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 Apr 8, 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**: Medline Convenience kits labeled as: 1) MINOR BASIC PACK-LF, Pack Number DYNJ0281516M; 2) MINOR ACUTE PACK-LF, Pack Number DYNJ0484979B
- **Reason**: Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
- **Classification**: Class II
- **Recalling firm**: MEDLINE INDUSTRIES, LP - Northfield
- **Quantity**: Not supplied
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-3025-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3025-2024%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 | DYNJ0281516M , Lot Number 19EBW985 ; DYNJ0281516M , Lot Number 19FBS033 ; DYNJ0281516M , Lot Number 19GBE356 ; DYNJ0281516M , Lot Number 19GBN481 ; DYNJ0281516M , Lot Number 19SBC273 ; DYNJ0281516M , Lot Number 19VBH540 ; DYNJ0281516M , Lot Number 19LBS319 ; DYNJ0281516M , Lot Number 20ABZ597 ; DYNJ0281516M , Lot Number 20DBH983 ; DYNJ0281516M , Lot Number 20FBJ183 ; DYNJ0281516M , Lot Number 20HBK308 ; DYNJ0281516M , Lot Number 20JBZ789 ; DYNJ0281516M , Lot Number 20LBU288 ; DYNJ0281516M , Lot Number 21CBD769 ; DYNJ0281516M , Lot Number 21EMF053 ; DYNJ0281516M , Lot Number 21GMB207 ; DYNJ0281516M , Lot Number 21HMD725 ; DYNJ0281516M , Lot Number 21IMF128 ; DYNJ0281516M , Lot Number 21LMC143 ; DYNJ0281516M , Lot Number 22AMF940 ; DYNJ0281516M , Lot Number 22CMC800 ; DYNJ0281516M , Lot Number 22CMD981 ; DYNJ0281516M , Lot Number 22EMG839 ; DYNJ0281516M , Lot Number 22EMH435 ; DYNJ0281516M , Lot Number 22HMC805 ; DYNJ0281516M , Lot Number 22JMA630 ; DYNJ0281516M , Lot Number 22LMA629 ; DYNJ0281516M , Lot Number 23AMB717 ; DYNJ0281516M , Lot Number 23BMI443 ; DYNJ0281516M , Lot Number 23DMG317 ; DYNJ0281516M , Lot Number 23FMC971 ; DYNJ0281516M , Lot Number 23GMD118 ; DYNJ0281516M , Lot Number 23HMH453 ; DYNJ0281516M , Lot Number 23JMB170 ; DYNJ0281516M , Lot Number 23KME384 ; DYNJ0281516M , Lot Number 19AKA641 ; DYNJ0281516M , Lot Number 19BKD684 ; DYNJ0281516M , Lot Number 19DKC345 ; DYNJ0484979B , Lot Number 18LBO447 ; DYNJ0484979B , Lot Number 19CBU327 |

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**: Sep 18, 2024
- **Recall initiation date**: Apr 8, 2024
- **Center classification date**: Sep 6, 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-3025-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [MEDLINE INDUSTRIES, LP - Northfield records](https://isitonrecall.com/brand/medline-industries-lp-northfield/)