Medical Device Recalls
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1 result found
Recall Number: Z-2202-2016 |
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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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| Femoral Arterial Line Catheterization Kit with Sharps Safety Features 510K 810675, product code DQ... | 2 | 07/12/2016 |
FEI # 3015859709 Arrow International Inc |
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