Medical Device Recalls
-
|
1 to 5 of 5 Results
510(K) Number: K152944 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Hillrom Welch Allyn Q-Stress Cardiac Stress Testing System; cardiac stress test | 2 | 11/07/2024 |
FEI # 1417572 Baxter Healthcare Corporation |
| Hillrom Welch Allyn XScribe Cardiac Stress Testing System; Programmable Diagnostic Computer | 2 | 11/07/2024 |
FEI # 1417572 Baxter Healthcare Corporation |
| XScribe Cardiac Stress Testing System, version 6, with below product names and codes: a) XS6/RS6 REV... | 2 | 01/10/2024 |
FEI # 1417572 Baxter Healthcare Corporation |
| Q-Stress Cardiac Stress Testing System, version 6, with below product name / product codes: a) QS6 A... | 2 | 01/10/2024 |
FEI # 1417572 Baxter Healthcare Corporation |
| Q-Stress/XScribe. Q-Stress or XScribe is a diagnostic device capable of real time ECG display, heart... | 2 | 04/29/2020 |
FEI # 2183461 WELCH ALLYN, INC/MORTARA |
-







