Medical Device Recalls
-
1 result found
510(K) Number: K170144 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Philips Allura (Model Numbers 722010, 722012, 722026, 722027, 722028, 722029, 722035) and Philips Az... | 2 | 04/06/2022 | Philips North America Llc |
-