Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
5Fr PowerPICC Catheter Single-Lumen with 70cm Guidewire Instructions For Use: Recalled by Bard Access Systems Inc. Due to Catheter kits contained the incorrect micro-introducers.
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
5Fr PowerPICC Catheter Single-Lumen with 70cm Guidewire Instructions For Use: PowerPicc Polyurethand Radiology PiCC with Microintroducer
Quantity: 180 units
Why Was This Recalled?
Catheter kits contained the incorrect micro-introducers.
Where Was This Sold?
This product was distributed to 10 states: CT, GA, MA, MI, MT, NV, NJ, NY, VA, WI
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