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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
Related Medical Device Recalls
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Z-1393-2017 - TriForce Peripheral Crossing Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. The TriForce Peripheral Crossing Set is intended to be percutaneously introduced into blood ... 2 03/02/2017 FEI # 1820334
Cook Inc.
Z-1391-2017 - Micropuncture Check-Flo Performer Introducer Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapere... 2 03/02/2017 FEI # 1820334
Cook Inc.
Z-1390-2017 - Flexor Radial Access Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. The Flexor® Radial Hydrophilic Introducer Access Set is intended to introduce diagnostic and interve... 2 03/02/2017 FEI # 1820334
Cook Inc.
Z-1387-2017 - Check-Flo Performer Introducer, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end catheters or... 2 03/02/2017 FEI # 1820334
Cook Inc.
Z-1388-2017 - Check-Flo Performer Introducer Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end catheter... 2 03/02/2017 FEI # 1820334
Cook Inc.
Z-1392-2017 - Check-Flo Introducer Hausdorf-Lock Atrial, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end c... 2 03/02/2017 FEI # 1820334
Cook Inc.
Z-1389-2017 - Check-Flo Hemostasis Assembly, Individual product is packaged in a Tyvek-film sterilizable outer pouch. 2 03/02/2017 FEI # 1820334
Cook Inc.
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