Reported Jun 14, 2023 · Ongoing
Magic3 Go Intermittent Urinary Catheters, pediatric Catalog Numbers: a) REF 52810G
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?
- Magic3 Go Intermittent Urinary Catheters
- pediatric Catalog Numbersa) REF 52810G
- Lot codes and dates
a) REF 52810GUDI/DI 00801741136870
- Lot NumbersJUGW1445
- Amount recalled
- 5760 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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