Medical Device Recalls
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21 to 22 of 22 Results
510(K) Number: K830755 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Arrow 4way Hi-Flo Stopcock with male luer lock, latex free used in various IV kits. | 2 | 06/24/2009 | Arrow International Inc |
Arrow Extension sets and accessories for intravascular use. | 2 | 06/24/2009 | Arrow International Inc |
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