medical Class II Updated 2019-09-04

Bard Peripheral Vascular Inc recalls GlidePath Long-Term Hemodialysis Catheter with Preloaded sty

Recalled Product

GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet, REF/Product code:5397230, 14.5F, straight, 23cm length, BARD, UDI: 00801741012303

Hazard / Issue

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.

Issued by

FDA

Affected States: 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, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY

Lot/Code Info: (Lot #, Exp.) REDN4412 12/31/2020; RECZ0753 3/31/2020; RECW0970 3/31/2020; RECW0387 6/30/2020

View official government recall

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