Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K874063 |
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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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| Description/REF: PARACENTESIS KIT/ASK-00376-JHH | 1 | 06/13/2026 |
FEI # 3013162291 ARROW INTERNATIONAL, LLC |
| Maximal Barrier Drape; Product Codes: ASK-00376-SU | 2 | 05/30/2018 |
FEI # 3015859709 Arrow International Inc |
| Large Volume Abdominal Paracentesis Kit | 2 | 04/03/2018 |
FEI # 3015859709 Arrow International Inc |
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