Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K050310 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
BardPort Titanium Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter , R... | 2 | 03/26/2020 | Bard Peripheral Vascular Inc |
BardPort Titanium Implanted Port. Bard Access Systems. Assembled in Mexico. A totally implantab... | 3 | 09/08/2011 | Bard Access Systems |
-