Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with Recalled by Bard Access Systems Inc. Due to Catheter convenience kits contain the incorrect guidewire. Kits...
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 Bard Access Systems Inc. directly.
Affected Products
5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with 70 cm Guidewire Unit Label: PowerPICC REF CK000340B BARD MYPICC KIT 5F French Size Dual-Lumen 70cm Guidewire
Quantity: 30 kits
Why Was This Recalled?
Catheter convenience kits contain the incorrect guidewire. Kits were labeled with 70cm guidewires, but contained a 50cm guidewire.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bard Access Systems Inc.
Bard Access Systems Inc. has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report