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Bard Peripheral Vascular Inc recalls PowerPort isp M.R.I. Implantable Port with Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter
Recalled December 4, 2019 · FDA recall Z-0582-2020 · Bard Peripheral Vascular
Hazard
Complaints received that products packaged with the incorrect introducer sheath size. · FDA Class II
Units
900 units
Sold at
US - Nationwide OUS - None
Description
Complaints received that products packaged with the incorrect introducer sheath size.
Product
PowerPort isp M.R.I. Implantable Port with Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter
Manufacturer(s)
Bard Peripheral Vascular Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →