FDA Device recall Z-2371-2019

EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet, REF/Product code:5903190, 14.5F, Straight ,19cm length, BARD, UDI# 0080174…

FDA Device
Class II
terminated
Published 2019-09-04

On 2019-09-04 the FDA classified a Class II recall of EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet, REF/Product code:5903190, 14.5F, Straight ,19cm length, BARD, UDI# 0080174… by Bard Peripheral Vascular, citing 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.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2371-2019
Classification	Class II
Status	terminated
Initiated	2019-05-31
Published	2019-09-04
Last updated	2026-09-13 11:55 UTC
Company	Bard Peripheral Vascular
Distribution	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, VT, WA, WI, WV, WY

Product

EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet, REF/Product code:5903190, 14.5F, Straight ,19cm length, BARD, UDI# 00801741013690

Reason

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.

Identifiers

code_info	(Lot #, Exp.) RECZ3009 8/31/2020 RECZ0716 7/31/2020 RECW0585 7/31/2020 RECX1187 8/31/2020 RECV1624 1/31/2020

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2371-2019%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.