[Recalled] Bard Foley procedural trays packaged in breather bags. The product is packaged ten units in each shipper box, and are sold sterile for single use. Used to catheterize patients. The finished trays are sold in Tyvek breather ba
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Bard Foley procedural trays packaged in breather bags. The product is packaged ten units in each shipper box, and are sold sterile for single use. Used to catheterize patients. The finished trays are sold in Tyvek breather bags. |
|---|---|
| Brand / manufacturer | C.R. Bard, Inc., Urological Division |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2327-2012 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 29 June 2012 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Incomplete seal on sterile packages of product.
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 →
Related recalls from C.R. Bard, Inc., Urological Division
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.
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