---
title: "Medline medical convenience kits labeled as: NEURO PACK, Medline Kit SKU DYNJ... — FDA record Z-2790-2026 | Is It on Recall"
description: "Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacill"
url: https://isitonrecall.com/recall/fda-device-z-2790-2026-medline-medical-convenience-kits-labeled-as-neuro-pack-medline-kit-sku-dynj59397p/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Medline medical convenience kits labeled as: NEURO PACK, Medline Kit SKU DYNJ59397P — FDA record Z-2790-2026

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 11, 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 medical convenience kits labeled as: NEURO PACK, Medline Kit SKU DYNJ59397P
- **Reason**: Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species.
- **Classification**: Class II
- **Recalling firm**: Medline Industries, LP
- **Quantity**: 574 kits
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2790-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2790-2026%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 | UDI/DI 10198459098109 (each) 40198459098100 (case), Lot Numbers: 25AMJ225, 25CMF838, 24KME164, 25DMB248, 25FMD941, 25GMB662, 25GMG296. |

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

## Distribution

US: CT, FL, KS, OH, OR, NY, MD, MT, VA, MA.

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

- [Connecticut](https://isitonrecall.com/state/connecticut/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Kansas](https://isitonrecall.com/state/kansas/)
- [Massachusetts](https://isitonrecall.com/state/massachusetts/)
- [Maryland](https://isitonrecall.com/state/maryland/)
- [Montana](https://isitonrecall.com/state/montana/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Oregon](https://isitonrecall.com/state/oregon/)
- [Virginia](https://isitonrecall.com/state/virginia/)

## Dates in the source

- **Report date**: Jul 29, 2026
- **Recall initiation date**: Jun 11, 2026
- **Center classification date**: Jul 23, 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-2790-2026%22)

## Related records

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