Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Magic3 Go Intermittent Urinary Catheters Recalled by C.R. Bard Inc Due to Some catheters had a manufacturing defect where the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact C.R. Bard Inc directly.
Affected Products
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
Quantity: 7427880 devices
Why Was This 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.
Where Was This Sold?
Worldwide
About C.R. Bard Inc
C.R. Bard Inc has 65 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report