[Recalled] Magic3 Intermittent Catheter with Sure Grip Hydrophilic Coated Silicone Coude tip, Product Code 50614. The catheters are packaged in film-to-film pouches and packaged 30 per box. Used as an Intermittent Urinary Catheter — Pote
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Magic3 Intermittent Catheter with Sure Grip Hydrophilic Coated Silicone Coude tip, Product Code 50614. The catheters are packaged in film-to-film pouches and packaged 30 per box. Used as an Intermittent Urinary Catheter |
|---|---|
| Brand / manufacturer | C.R. Bard, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2732-2015 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 24 August 2015 |
| EAN / barcode | 53621456 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Potential breach of the sterile barrier packaging.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
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This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.