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C.R. Bard Inc recalls Magic3 Go Intermittent Urinary Catheters, Female Catalog Numbers: a) REF 51808, b) REF 51810, c) REF 51812, d) REF 51814
Recalled June 14, 2023 · FDA recall Z-1698-2023 · C.R. Bard
Hazard
Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that could impact product sterility. · FDA Class II
Units
9894922 devices
Sold at
Worldwide
Description
Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that could impact product sterility.
Product
Magic3 Go Intermittent Urinary Catheters, Female Catalog Numbers: a) REF 51808, b) REF 51810, c) REF 51812, d) REF 51814, e) REF 51816, f) REF 51818
Manufacturer(s)
C.R. Bard Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →