Reported May 26, 2021 · Terminated
REF 7655405, Groshong NXT ClearVue Catheter, Basic Kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741035279 - Product…
Bard Access Systems 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 Access Systems Inc. · 605 N 5600 W · Salt Lake City, UT · 84116-3738
Is this the product you have?
- REF 7655405, Groshong NXT ClearVue Catheter, Basic Kit, 4F, Single-Lumen, 60 cm
- UDI(01)10801741035279 -
- Product Usageis designed for use when central venous catheterization is prescribed
- Lot codes and dates
- Lot No.
83 of 83 codes
reds2369reds3369reds4464reds4588redt0655redt0787redt1710redt1760redt2668redt2909redt4286redt4309redu0080redu0745redu0826redu0827redu1375redu1533redu2186redu2403redu2995redu3073redu3829redu3920redv1130redv1285REDV2022redv2095redv2812redv2886redv3944REDV4092REDW0350REDW0460redw1019redw1151redw1668redw1669redw1695redw2471redw2592redw3754redx0981redx0982redx0984redx0985redx0986redx0987redx1000redx1001REDX1002redx1003redx4676redy0095redy0096redy0108redy0109redy0644redy0703REDZ0125
- Lot No.
- Amount recalled
- N/A
This recall covers 18 products
The agency filed one notice per product. You are reading one of them; the other 17 are below.
5 more are in the archive.
Where it was sold
Why it was recalled
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
This product could cause temporary or reversible health problems — stop using it.
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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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