Reported Jun 14, 2023 · Ongoing
Magic3 Go Intermittent Urinary Catheters, male Catalog Numbers: a) REF 50810G, b) REF 50812G, c) REF 50814G, d) REF…
C.R. Bard 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: C.R. Bard Inc · 8195 Industrial Blvd Ne · Covington, GA · 30014-1497
Is this the product you have?
11 of 11 products
| Model / number | Product as published |
|---|---|
50810G | — |
50812G | — |
50814G | — |
50816G | — |
50818G | — |
53810G | — |
53812G | — |
53814G | — |
53816G | — |
53818G | — |
53820G | — |
- Amount recalled
- 7427880 devices
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Why it was recalled
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.
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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