Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Bard Foley procedural trays packaged in breather bags. The product Recalled by C.R. Bard, Inc., Urological Division Due to Incomplete seal on sterile packages of product.
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., Urological Division directly.
Affected Products
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.
Quantity: 56,694 units
Why Was This Recalled?
Incomplete seal on sterile packages of product.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About C.R. Bard, Inc., Urological Division
C.R. Bard, Inc., Urological Division has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report