FDA Device recall Z-1938-2015
EXPRESS Dry Seal Chest Drain, Single Collection P/N: 4000-100N
- FDA Device
- Class II
- terminated
- Published 2015-07-08
On 2015-07-08 the FDA classified a Class II recall of EXPRESS Dry Seal Chest Drain, Single Collection P/N: 4000-100N by Atrium Medical, citing chest drains have a missing o-ring.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1938-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-05-07 |
| Published | 2015-07-08 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Atrium Medical |
| Distribution | US |
Product
EXPRESS Dry Seal Chest Drain, Single Collection P/N: 4000-100N
Reason
Chest drains have a missing o-ring
Identifiers
| code_info | Lot Number: 222516 |
|---|
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-1938-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.