Atrium Express Dry Seal ATS — Class II medical device recall Z-0743-2014
Terminated recall by Atrium Medical Corporation, reported 2014-01-22, distributed nationwide. Chest Drain tubing of of the ATS Blood recovery may leak or disconnect
| Recall number | Z-0743-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Atrium Medical Corporation, Hudson, NH, United States |
| Recall initiated | 2013-11-19 |
| Classified | 2014-01-14 |
| Reported by FDA | 2014-01-22 |
| Terminated | 2015-06-11 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, CA, CO, IE, JO, LB, NL, RO, RU, TW, ZA |
| Quantity | 1,944 units |
| Reason classes | packaging |
| Lot numbers | 10913346 |
Product
Atrium Express Dry Seal ATS (Autotransfusion) Blood Recovery System Chest Drain with Prefilled Air Leak Monitor; Product Code: 4050-100P. To evacuate air and/or fluid from the chest cavity or mediastinum.
Reason for recall
Chest Drain tubing of of the ATS Blood recovery may leak or disconnect
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-0743-2014. 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.