FDA Device recall Z-0743-2014
Atrium Express Dry Seal ATS (Autotransfusion) Blood Recovery System Chest Drain with Prefilled Air Leak Monitor
- FDA Device
- Class II
- terminated
- Published 2014-01-22
On 2014-01-22 the FDA classified a Class II recall of Atrium Express Dry Seal ATS (Autotransfusion) Blood Recovery System Chest Drain with Prefilled Air Leak Monitor by Atrium Medical, citing chest Drain tubing of of the ATS Blood recovery may leak or disconnect.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0743-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-11-19 |
| Published | 2014-01-22 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Atrium Medical |
| Distribution | US |
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
Chest Drain tubing of of the ATS Blood recovery may leak or disconnect
Identifiers
| code_info | Lot number starting with 10883097 and the ending lot number 10913346 (All units in between and including these two numbers) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0743-2014%22
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