Medical Device Recalls
-
|
1 to 4 of 4 Results
510(K) Number: K152980 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Acumen IQ Sensor, REFs: AIQS6, AIQS65, AIQS6R, AIQS6R5, AIQS8, AIQS85, AIQS8R5, Rx only, Sterile EO.... | 2 | 11/29/2023 |
FEI # 2015691 Edwards Lifesciences, LLC |
| FloTrac Sensor with Vamp System, REF: MHD6AZ, MHD6AZ5 , MHD6C502 STIRLEEO, Rx only. For use in intra... | 2 | 11/29/2023 |
FEI # 2015691 Edwards Lifesciences, LLC |
| FloTrac Sensor, REF: MHD8 & MHD85,MHD6R5, MHD8R, MHD8R5, MHD8S, STERILEEO, Rx only. For use in intra... | 2 | 11/29/2023 |
FEI # 2015691 Edwards Lifesciences, LLC |
| Acumen IQ Sensor with VAMP System, REFs: AIQS6AZ & AIQS6AZ5, STERILEEO, Rx only. For use in intravas... | 2 | 11/29/2023 |
FEI # 2015691 Edwards Lifesciences, LLC |
-







