Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K040636 |
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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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| Smiths Medical CADD Medication Cassette Reservoir with clamp and female Luer. Nonvented stopper inc... | 2 | 09/04/2025 |
FEI # 3012307300 ICU Medical Inc. |
| CADD Administration Set, List Numbers: 1) REF 21-7300-24, 2) REF 21-7301-24 3) REF 21-7302-24, 4)... | 1 | 01/30/2023 |
FEI # 3012307300 Smiths Medical ASD Inc. |
| CADD® Administration Set, 21-7339-24, Rx Only, Sterile EO. | 2 | 03/30/2017 |
FEI # 3012307300 Smiths Medical ASD Inc. |
| CADD Administration Sets with Flow Stop, Product Reorder No: 21-7321-01, 21-7321-24, 21-7322-01, 21... | 2 | 05/27/2016 |
FEI # 2183502 Smiths Medical ASD, Inc. |
| Smiths CADD Yellow Medication Cassette Reservoirs with Flow Stop, Clamp and Female Luer, 100 ml, Reo... | 2 | 02/13/2008 |
FEI # 2183502 Smiths Medical MD, Inc. |
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