Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K943897 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| 1050 STOPCOCK LEFT ROTATOR OFF HANDLE, List Number MX1431MRL | 2 | 01/17/2024 |
FEI # 1526863 Smiths Medical Asd Inc |
| 6IN PRESSURE TUBING, List Number MX20617 | 2 | 01/17/2024 |
FEI # 1526863 Smiths Medical Asd Inc |
| Medex 700PSI STOPCOCK W/ROTATOR, List Number MX4331R | 2 | 01/17/2024 |
FEI # 1526863 Smiths Medical Asd Inc |
| 48IN (121.9CM) INJ LINE ROTATING ADAPT (900psi), List Number MX694R | 2 | 01/17/2024 |
FEI # 1526863 Smiths Medical Asd Inc |
| HIGH PRESSURE ROTATOR WITH FEMALE LUER LOCK, List Number MX497HP | 2 | 01/17/2024 |
FEI # 1526863 Smiths Medical Asd Inc |
| Medex 20IN (50.8CM) INJ LINE ROTATING ADAPT, List Number MX682R | 2 | 01/17/2024 |
FEI # 1526863 Smiths Medical Asd Inc |
| HIGH PRESSURE ROTATOR WITH MALE LUER LOCK, List Number MX496HP | 2 | 01/17/2024 |
FEI # 1526863 Smiths Medical Asd Inc |
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