Reported Sep 4, 2019 · Terminated
GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5393230, 14.5F, Straight, 23cm…
Bard Peripheral Vascular Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Bard Peripheral Vascular Inc · 1625 W 3rd St Bldg 1 · Tempe, AZ · 85281-2438
Is this the product you have?
- GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet
- REF/Product code
539323014.5FStraight23cm lengthBARD
- UDI00801741012181
- Lot codes and dates
13 of 13 products
Products covered by this recall # Product as published 1 (Lot #, Exp.) REDN1423 8/31/2020 2 REDN0141 4/30/2020 3 RECZ2974 8/31/2020 4 RECZ0639 3/31/2020 5 RECZ1098 3/31/2020 6 RECY7435 3/31/2020 7 RECX2895 3/31/2020 8 RECX1714 4/30/2020 9 RECX0653 3/31/2020 10 RECW2371 4/30/2020 11 RECW1714 6/30/2020 12 RECX0998 7/31/2020 13 RECV2487 8/31/2020 - Amount recalled
- 10,507 units
This recall covers 28 products
The agency filed one notice per product. You are reading one of them; the other 27 are below.
15 more are in the archive.
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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