Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K073451 |
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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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PICC Kits with Peel-Away Sheath Component; catheter, intravascular, therapeutic, ultrasound Produ... | 2 | 08/25/2015 | Arrow International Inc |
Arrow Select Kits (ASK) and Maximal Barrier Precautions Kits (CDC) with BD Medical Posiflush 10mL Sa... | 2 | 10/14/2014 | Arrow International Inc |
Arrow International, Inc. PICC Kits and VPS Access Kits with Touhy Borst Component Catheter, Intrava... | 2 | 08/31/2015 | Arrow International Inc |
Arrow ErgoPack Pressure Injectable One-Lumen PICC, REF CDC-05541-HPK1A; catheter, intravascular | 2 | 09/15/2023 | ARROW INTERNATIONAL Inc. |
Arrow 4FR Peripherally Inserted Central Catheter (PICCs) Kits. Product numbers: ASK-01451-BMH; ASK-... | 2 | 05/26/2010 | Arrow International Inc |
4FR Single Lumen Pressure Injectable PICC; intravascular therapeutic catheter, for long-term use gr... | 2 | 10/15/2015 | Arrow International Inc |
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