Medical Device Recalls
-
1 to 5 of 5 Results
510(K) Number: K040636 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
CADD Administration Set, List Numbers: a) REF 21-7300-24, b) REF 21-7301-24, c) REF 21-7302-24, ... | 1 | 01/30/2023 | Smiths Medical ASD Inc. |
CADD® Administration Set, 21-7339-24, Rx Only, Sterile EO. | 2 | 03/30/2017 | 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 | Smiths Medical ASD, Inc. |
CADD" Medication Cassette Reservoir, 50mL, REF 21-7001-24 & 21-7301-24, Sterile EO, Rx only. | 2 | 03/17/2015 | Smiths Medical ASD, Inc. |
Smiths CADD Yellow Medication Cassette Reservoirs with Flow Stop, Clamp and Female Luer, 100 ml, Reo... | 2 | 02/13/2008 | Smiths Medical MD, Inc. |
-