Bard Peripheral Vascular Inc: Medical Device Recall in 2019 - (Recall #: Z-0582-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

PowerPort isp M.R.I. Implantable Port with Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter

Product Classification:

Class II

Date Initiated: February 14, 2019

Date Posted: December 4, 2019

Recall Number: Z-0582-2020

Event ID: 84169

Reason for Recall:

Complaints received that products packaged with the incorrect introducer sheath size.

Status: Ongoing

Product Quantity: 900 units

Code Information:

Product Code: 1808060 Device Listing Number: D004935 UDI: (01)00801741027031(17)191130(10)RECS2407 Lot Number: RECS2407

Distribution Pattern:

US - Nationwide OUS - None

Voluntary or Mandated:

Voluntary: Firm initiated