Bard Access Systems Inc.: Medical Device Recall in 2021 - (Recall #: Z-1994-2021)

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:

5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with 70 cm Guidewire Unit Label: PowerPICC REF CK000340B BARD MYPICC KIT 5F French Size Dual-Lumen 70cm Guidewire

Product Classification:

Class II

Date Initiated: May 19, 2021

Date Posted: July 7, 2021

Recall Number: Z-1994-2021

Event ID: 88057

Reason for Recall:

Catheter convenience kits contain the incorrect guidewire. Kits were labeled with 70cm guidewires, but contained a 50cm guidewire.

Status: Terminated

Product Quantity: 30 kits

Code Information:

Catalog (REF) Number: CK000340B UDI Code: (01)00801741126697 Lot Number: 20BBK658

Distribution Pattern:

U.S. Nationwide distribution in the state of RI.

Voluntary or Mandated:

Voluntary: Firm initiated