Medical Device Recalls
-
|
1 result found
510(K) Number: K013243 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| PROLARYN PLUS Injectable Implant 1.0 cc Plus Calcium Hydroxlyapatite (CaHA) Injectable Implant, Mode... | 2 | 12/03/2015 | Merz North America, Inc. |
-







