---
title: "Namic Preceptor Manifold, custom, Medline Product Number/SKU 64039307; Extrav... — FDA record Z-2142-2026 | Is It on Recall"
description: "Medline has identified the presence of particulate within the fluid path of the Manifolds."
url: https://isitonrecall.com/recall/fda-device-z-2142-2026-namic-preceptor-manifold-custom-medline-product-number-sku-64039307-extravascular-blood-pressure-tra/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Namic Preceptor Manifold, custom, Medline Product Number/SKU 64039307; Extravascular blood pressure transducer — FDA record Z-2142-2026

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 Mar 24, 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**: Namic Preceptor Manifold, custom, Medline Product Number/SKU 64039307; Extravascular blood pressure transducer
- **Reason**: Medline has identified the presence of particulate within the fluid path of the Manifolds.
- **Classification**: Class I
- **Recalling firm**: Medline Industries, LP
- **Quantity**: 760 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2142-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2142-2026%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 each 10193489059205, UDI/DI case 30193489059209, Lot Numbers: 117277, 119982, 122210, 122199, 130129, 133014, 136396, 138613, 139138, 157974, 162399, 164317, 175538, 193515, 193531. |

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

## Distribution

US (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK.

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

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## Dates in the source

- **Report date**: May 20, 2026
- **Recall initiation date**: Mar 24, 2026
- **Center classification date**: May 8, 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-2142-2026%22)

## Related records

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