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Bard Access Systems Inc. recalls PowerPICC Provena Catheters, as 3 Fr. Single lumen and 4 Fr. Dual Lumen. Packaged in a poly tray with Tyvek lid within
Recalled February 14, 2018 · FDA recall Z-0536-2018 · Bard Access Systems
Hazard
Possible leaks on the 3 Fr. Single lumen and 4 Fr. Dual lumen PowerPICC catheters at the luer hub extension leg junction. · FDA Class II
Units
53,699 units total
Sold at
Distribution US nationwide.
Description
Possible leaks on the 3 Fr. Single lumen and 4 Fr. Dual lumen PowerPICC catheters at the luer hub extension leg junction.
Product
PowerPICC Provena Catheters, as 3 Fr. Single lumen and 4 Fr. Dual Lumen. Packaged in a poly tray with Tyvek lid within a header bag configuration or a breather bag configuration.
Manufacturer(s)
Bard Access Systems Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →