Drug recall
Atrium Express Dry Seal Chest Drain ATS Blood Recovery, Catalog Number: 4050-100N. Autotransfusion Apparatus.
FDA recall event 68398 · Class II · Atrium Medical Corporation
Key facts
| Event ID | 68398 |
|---|---|
| Recall numbers | Z-1959-2014 |
| Recalling firm | Atrium Medical Corporation |
| Product type | Devices |
| Products | Atrium Express Dry Seal Chest Drain ATS Blood Recovery, Catalog Number: 4050-100N. Autotransfusion Apparatus. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Product that was previously recalled because the Chest Drain tubing of the ATS Blood recovery may leak or disconnect, was released for distribution in error. |
| Initiation date | Apr 28, 2014 |
| Report date | Jul 9, 2014 |
| Termination date | Mar 17, 2016 |
| City | Hudson |
| State | NH |
| Country | United States |
| FEI number | 1219977 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: