Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K153074 |
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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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| Kangaroo Connect 1000ml Bag Set, Non-Sterile, Product Code 77100FD - Product Usage: single-use tubin... | 2 | 11/13/2020 |
FEI # 3014524790 Cardinal Health 200, LLC |
| Kangaroo Connect 500ml Bag Set, Non-Sterile, Product Code 77500FD - Product Usage: single-use tubing... | 2 | 11/13/2020 |
FEI # 3014524790 Cardinal Health 200, LLC |
| Kangaroo Connect ENPlus Spike Set Anti-free Flow, Product Code 77000FD | 2 | 05/22/2020 |
FEI # 3004008697 Cardinal Health Inc. |
| Kangaroo Joey Safety Screw Spike Set, Anti-free Flow, Product Code 765559 | 2 | 05/22/2020 |
FEI # 3004008697 Cardinal Health Inc. |
| Kangaroo Joey Safety Screw Spike with Flush Bag, Anti-free Flow,1000 mL, Product Code 765100 | 2 | 05/22/2020 |
FEI # 3004008697 Cardinal Health Inc. |
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