Skip to content
Recall Observatory FDA recall evidence

Device product

EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet, REF/Product code:5903230, 14.5F, Straight ,23cm length, BARD, UDI: 00801741013706

Z-2372-2019

May 31, 2019

Class II

Product summary

Firm
Bard Peripheral Vascular Inc
Event
Event 83337
Status
Terminated
Classification
Class II
Quantity
1731 units
Official record key
device-enforcement:Z-2372-2019

Official wording

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.

Code information: (Lot #, Exp.) REDN2487 9/30/2020; RECX3053 3/31/2020; RECX0505 7/31/2020; RECW0964 7/31/2020; RECX1188 8/31/2020; RECV1544 1/31/2020; RECW0847 1/31/2020

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,

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.