FDA Device recall Z-0235-2023
Atrium Ocean Wet Suction Water Seal Chest Drain- Product Code: 2002-000
- FDA Device
- Class II
- ongoing
- Published 2022-11-23
On 2022-11-23 the FDA classified a Class II recall of Atrium Ocean Wet Suction Water Seal Chest Drain- Product Code: 2002-000 by Atrium Medical, citing warehouse experienced temperature excursions in July and August 2021. It was determined that there were no associated harms to patients.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0235-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-10-18 |
| Published | 2022-11-23 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Atrium Medical |
| Distribution | US |
Product
Atrium Ocean Wet Suction Water Seal Chest Drain- Product Code: 2002-000
Reason
Warehouse experienced temperature excursions in July and August 2021. It was determined that there were no associated harms to patients.
Identifiers
| code_info | UDI-DI: 20650862100017 - case / 00650862100013- each Lot Number: 472326, 473226 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0235-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.