---
title: "Fountain, REF: IS4-135-30 and IS4-90-10, CE2797, STERILEEO, Rx ONLY — FDA record Z-0629-2024 | Is It on Recall"
description: "The sterility of microcatheter and infusion system devices cannot be guaranteed."
url: https://isitonrecall.com/recall/fda-device-z-0629-2024-fountain-ref-is4-135-30-and-is4-90-10-ce2797-sterileeo-rx-only/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Fountain, REF: IS4-135-30 and IS4-90-10, CE2797, STERILEEO, Rx ONLY — FDA record Z-0629-2024

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 6, 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**: Fountain, REF: IS4-135-30 and IS4-90-10, CE2797, STERILEEO, Rx ONLY
- **Reason**: The sterility of microcatheter and infusion system devices cannot be guaranteed.
- **Classification**: Class II
- **Recalling firm**: Merit Medical Systems, Inc.
- **Quantity**: 3 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0629-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0629-2024%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 | REF: IS4-135-30 Lot # H2765720 UDI: 00884450000885 REF: IS4-90-10 Lot # H2765603 UDI: 00884450006504 |

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

## Distribution

Worldwide - US Nationwide distribution in the states of AL, AZ, CA, CO, CT, FL, IA, IL, IN, KS, MA, MD, MN, MO, NH, NJ, NSW, NV, NY, UT, WI and the countries of Argentina, Australia, Belgium, China, France, Germany, Guam, Hong Kong, Italy, Mexico, Netherlands, Switzerland.

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**: Jan 10, 2024
- **Recall initiation date**: Nov 6, 2023
- **Center classification date**: Jan 2, 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-0629-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Merit Medical Systems, Inc. records](https://isitonrecall.com/brand/merit-medical-systems-inc/)
