FDAApril 20, 2023device

Magic3 Go Intermittent Urinary Catheters, male Catalog Numbers: a) REF 50810G, b) REF 50812G, c) REF 50814G, d) REF 50816G, e) REF 50818G, f) REF 53810G, g) REF 53812G, h) REF 53814G, i) REF 53816G, j) REF 53818G, k) REF 53820G

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Ongoing

Brands named

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UPCs

08017411370060801741137013080174113702008017411370370801741137044080174113694808017411369550801741136962080174113697908017411369860801741136993

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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