Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K042126 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes | 2 | 09/30/2015 | Arrow International Inc |
PICC Kits with Peel-Away Sheath Component; catheter, intravascular, therapeutic, ultrasound Produ... | 2 | 08/25/2015 | Arrow International Inc |
Arrow Peripherally Inserted Central Catheter | 2 | 06/24/2009 | Arrow International Inc |
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