Medical Device Recalls
-
|
1 result found
510(K) Number: K950750 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| AC Power Adaptor (transformer), TENPAO Model U090100Q31; used with the Pump In Style Advanced family... | 2 | 05/27/2011 |
FEI # 1419937 Medela Inc |
-







