Medical Device Recalls
-
1 result found
Related Medical Device Recalls |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Z-1660-2014 - LIFEPAK 1000 defibrillator. Affected Part Numbers: 320371500XXX The LP1000 (in AED mode) is indicated for use on patients in cardiac arrest. | 2 | 05/23/2014 | Physio-Control, Inc. |
-