Bard Peripheral Vascular Inc: Medical Device Recall in 2021 - (Recall #: Z-1552-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 5829502, UDI: (01)00801741027406 - Product Usage: The port system can be used for infusion of medications, I.V. fluids, parenteral nutrition solutions, blood products, and for the withdrawal of blood samples.

Product Classification:

Class II

Date Initiated: March 25, 2021

Date Posted: May 19, 2021

Recall Number: Z-1552-2021

Event ID: 87656

Reason for Recall:

Catheters may experience difficulty in flushing, infusion, and/or aspiration, and septum dislodgements.

Status: Terminated

Product Quantity: 287 units

Code Information:

Code: REEV2356, REEX1383, REEX3996

Distribution Pattern:

US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN MO, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV.

Voluntary or Mandated:

Voluntary: Firm initiated