---
title: "External Drainage System Collection Bag, REF: NT821732C, STERILEEO, Rx only — FDA record Z-0634-2024 | Is It on Recall"
description: "Sterility assurance cannot be guaranteed for external drainage systems due to incomplete bioburden testing."
url: https://isitonrecall.com/recall/fda-device-z-0634-2024-external-drainage-system-collection-bag-ref-nt821732c-sterileeo-rx-only/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# External Drainage System Collection Bag, REF: NT821732C, STERILEEO, Rx only — FDA record Z-0634-2024

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 Nov 28, 2023. 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**: External Drainage System Collection Bag, REF: NT821732C, STERILEEO, Rx only
- **Reason**: Sterility assurance cannot be guaranteed for external drainage systems due to incomplete bioburden testing.
- **Classification**: Class II
- **Recalling firm**: Natus Medical Incorporated
- **Quantity**: 2,686 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0634-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0634-2024%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 | UDI: 00382830050562/ Lot #: 1FX0004951660 1FX0004951658 1FX0004951659 1FX0005040450 1FX0005040451 1FX0005040452 1FX0005040453 1FX0005040454 1FX0005040457 1FX0005040456 1FX0005079696 1FX0005126475 1FX0005126474 1FX0005040455 |

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

## Distribution

US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DC, FL, GA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV.

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

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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jan 10, 2024
- **Recall initiation date**: Nov 28, 2023
- **Center classification date**: Jan 4, 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-0634-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Natus Medical Incorporated records](https://isitonrecall.com/brand/natus-medical-incorporated/)
