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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K001901
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CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 CK000566 Poly Midl... 2 07/02/2026 FEI # 3006260740
Bard Access Systems, Inc.
BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: Bard Poly Midline 3F ... 2 03/13/2015 FEI # 3006260740
Bard Access Systems
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