Medical Device Recalls
-
|
1 to 3 of 3 Results
510(K) Number: K201305 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Express Dry Seal Chest Drains (Express): 4000-100N DRAIN, EXPRESS, SINGLE; 4050-100N DRAIN, EXPR... | 2 | 11/16/2023 |
FEI # 3011175548 Atrium Medical Corporation |
| Ocean Water Seal Chest Drains (Ocean): Products REF Number Product Name (1)2002-000 DRAIN, OCEAN ... | 2 | 11/16/2023 |
FEI # 3011175548 Atrium Medical Corporation |
| Product REF 4050-100N, DRAIN, EXPRESS BRU W/AC, Blood Recovery Unit | 1 | 01/12/2024 |
FEI # 2242352 Maquet Cardiovascular, LLC |
-







