Bard Peripheral Vascular Inc: Medical Device Recall in 2020 - (Recall #: Z-2209-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

EQUISTREAM¿ XK Long-Term Hemodialysis Catheter. REF/UDI:5913190/(01)00801741013836; 16F

Product Classification:

Class II

Date Initiated: June 14, 2019

Date Posted: June 10, 2020

Recall Number: Z-2209-2020

Event ID: 85510

Reason for Recall:

Incorrect Peel-Apart Introducer Sheath in Kit.

Status: Terminated

Product Quantity: 400

Code Information:

RECT0999

Distribution Pattern:

67 US Consignees. US - AL, AR, AZ, CA, FL, GA, IA, ID, IL, KY, LA, MD, MN, MT, NC, NY, OR, PA, TN, TX, VA, WA, WI and WV.

Voluntary or Mandated:

Voluntary: Firm initiated