Atrium Ocean Wet Suction Water Seal Chest Drain- Product Code:… — Class II medical device recall Z-0235-2023
Ongoing recall by Atrium Medical Corporation, reported 2022-11-23, distributed nationwide. Warehouse experienced temperature excursions in July and August 2021. It was determined that there were no ass
| Recall number | Z-0235-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Atrium Medical Corporation, Merrimack, NH, United States |
| Recall initiated | 2022-10-18 |
| Classified | 2022-11-15 |
| Reported by FDA | 2022-11-23 |
| Distributed | Nationwide (US) |
| Reason classes | temperature control |
| UPC / GTIN / UDI-DI | 20650862100017 |
| Lot numbers | 472326, 473226 |
Product
Atrium Ocean Wet Suction Water Seal Chest Drain- Product Code: 2002-000
Reason for recall
Warehouse experienced temperature excursions in July and August 2021. It was determined that there were no associated harms to patients.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0235-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.