Atrium Express Dry Seal Chest Drain ATS Blood Recovery — Class II medical device recall Z-1959-2014
Terminated recall by Atrium Medical Corporation, reported 2014-07-09, distributed in AK, CA, MD, MN, MO, NC, NJ, OH…. Product that was previously recalled because the Chest Drain tubing of the ATS Blood recovery may leak or disc
| Recall number | Z-1959-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Atrium Medical Corporation, Hudson, NH, United States |
| Recall initiated | 2014-04-28 |
| Classified | 2014-07-01 |
| Reported by FDA | 2014-07-09 |
| Terminated | 2016-03-17 |
| Distributed | AK, CA, MD, MN, MO, NC, NJ, OH, UT |
| Reason classes | packaging |
| Lot numbers | 10906458 |
| Model numbers | 4050-100N |
Product
Atrium Express Dry Seal Chest Drain ATS Blood Recovery, Catalog Number: 4050-100N. Autotransfusion Apparatus.
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.
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-1959-2014. 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.