Bard Peripheral Vascular Inc: Medical Device Recall in 2019 - (Recall #: Z-2385-2019)

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:

GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5393270, 14.5F, Straight, 27cm length, BARD, UDI: 00801741012198

Product Classification:

Class II

Date Initiated: May 31, 2019

Date Posted: September 4, 2019

Recall Number: Z-2385-2019

Event ID: 83337

Reason for Recall:

The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.

Status: Terminated

Product Quantity: 2,298 units

Code Information:

(Lot #, Exp.) REDN4346 9/30/2020; RECZ2996 7/31/2020; RECX1128 3/31/2020; RECX1122 8/31/2020; RECX1195 3/31/2020

Distribution Pattern:

US: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA,MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VI, VT, WA, WI, WV, WY OUS: Australia, Canada,

Voluntary or Mandated:

Voluntary: Firm initiated