Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K991088 |
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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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| BD Vacutainer Luer-Lok Access Device Holder with Pre-Attached Multiple Sample Adapter Sterile, Do ... | 2 | 12/06/2006 |
FEI # 2243072 Becton Dickinson & Company |
| BD Vacutainer Luer Adapter; Catalog #367290 and #367300. | 2 | 09/09/2006 |
FEI # 2243072 Becton Dickinson & Company |
| Regard Custom Procedure Kits containing BD Luer Lok Access Devices | 3 | 03/30/2022 |
FEI # 3014527682 ROi CPS LLC |
| BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide ... | 3 | 02/23/2022 |
FEI # 2243072 Becton Dickinson & Company |
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