---
title: "Atrium Oasis Dry Suction Water Seal Chest Drain, Part Number: 3600-100, DRAIN... — FDA record Z-0485-2024 | Is It on Recall"
description: "Product was re-processed and re-sterilized by a third party using packaging configurations and a sterilization process which are not approved by the manufacture"
url: https://isitonrecall.com/recall/fda-device-z-0485-2024-atrium-oasis-dry-suction-water-seal-chest-drain-part-number-3600-100-drain-oasis-single-w-ac-3600-si/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Atrium Oasis Dry Suction Water Seal Chest Drain, Part Number: 3600-100, DRAIN, OASIS SINGLE W/AC, 3600 SINGLE COLLECT... — FDA record Z-0485-2024

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 Sep 5, 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**: Atrium Oasis Dry Suction Water Seal Chest Drain, Part Number: 3600-100, DRAIN, OASIS SINGLE W/AC, 3600 SINGLE COLLECTION.
- **Reason**: Product was re-processed and re-sterilized by a third party using packaging configurations and a sterilization process which are not approved by the manufacture and lack validation.
- **Classification**: Class II
- **Recalling firm**: Atrium Medical Corporation
- **Quantity**: Not supplied
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0485-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0485-2024%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-DI: 20650862110016. Lots: 460793, 461324, 463567, 463568, 463569, 466447, 466945, 466946, 467473, 467843, 471055, 471797, 472571, 474505, 477919, 480204, 480205, 480658, 482038, 483030, 483794, 484519, 484521, 484530, 486156, 486531, 487059, 488305, 489762. |

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

## Distribution

US: VA

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

- [Virginia](https://isitonrecall.com/state/virginia/)

## Dates in the source

- **Report date**: Dec 13, 2023
- **Recall initiation date**: Sep 5, 2023
- **Center classification date**: Dec 1, 2023

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-0485-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Atrium Medical Corporation records](https://isitonrecall.com/brand/atrium-medical-corporation/)