Bard Access Systems Inc.: Medical Device Recall in 2021 - (Recall #: Z-1991-2021)

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:

5Fr PowerPICC Catheter Single-Lumen with 70cm Guidewire Instructions For Use: PowerPicc Polyurethand Radiology PiCC with Microintroducer

Product Classification:

Class II

Date Initiated: May 19, 2021

Date Posted: July 7, 2021

Recall Number: Z-1991-2021

Event ID: 88048

Reason for Recall:

Catheter kits contained the incorrect micro-introducers.

Status: Terminated

Product Quantity: 180 units

Code Information:

Catalog Number: 3175155 UDI Code: (01)00801741027680 Lot Number: REEU0201

Distribution Pattern:

U.S.: CT, GA, MA, MI, MT, NJ, NV, NY, VA, and WI. O.U.S.: None

Voluntary or Mandated:

Voluntary: Firm initiated