Medical Device Recalls
-
|
1 to 3 of 3 Results
510(K) Number: K905235 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit) | 1 | 01/17/2024 |
FEI # 1000524541 Percussionaire Corporation |
| Monitron II Waveform Analyzer, REF: S00015-1, used with ventilators. | 2 | 11/07/2023 |
FEI # 1000524541 Percussionaire Corporation |
| VDR4 Phasitron Breathing Circuit Models that contain the venturi component: -A50094 D 5PK, Phasitro... | 1 | 01/23/2025 |
FEI # 1000524541 Percussionaire Corporation |
-







