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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-2667-2026
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CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770 S4153108BDP Proven... 2 07/02/2026 FEI # 3006260740
Bard Access Systems, Inc.
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