Reported Jun 14, 2023 · Ongoing
HydroSil Go Intermittent Urinary Catheters, Catalog Numbers: a) REF 71808, b) REF 71810, c) REF 71812, d) REF 71814, e)…
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?
- HydroSil Go Intermittent Urinary Catheters
- Catalog Numbers
a) REF 71808b) REF 71810c) REF 71812d) REF 71814e) REF 71816f) REF 71818
- Lot codes and dates
6 of 6 products
Products covered by this recall Model / number Product as published 71808Lot Numbers: JUGU9026 71810Lot Numbers: JUGT9154, JUGU9053, JUGV9130, JUGV9133 71812Lot Numbers: JUGT0236, JUGT1689, JUGT2702, JUGU1955, JUGU1968, JUGV9158 71814Lot Numbers: JUGT3326 71816Lot Numbers: JUGU9023 71818Lot Numbers: JUGT0288, JUGU9022 - Amount recalled
- 308520 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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