Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K932840 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Locator-Wand Cover that is sold in a shelf carton (unit packaging) separate to the sterile tray con... | 2 | 04/27/2006 | Smiths Medical MD, Inc. |
Port-A-Cath II Polysulfone/Titanium Venous Access System, with Silicone Catheter, 2.8mm O.D. x 1.0mm... | 2 | 07/20/2004 | Deltec, Inc |
-