Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot numbers and products inadvertently not included in...
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 Peripheral Vascular Inc directly.
Affected Products
Bard Biopsy EnCor Probe, MRI, 10G Trocar Tip, REF number ECPMR0110G, packaged individually in sterile pouches, 5 pouches/carton, Single Use, Rx, Sterile.
Quantity: 2,050 units
Why Was This Recalled?
Lot numbers and products inadvertently not included in the scope of the previous recall. Original recall was conducted due to an increase in probe failures for leaks, suction issues, and failure to obtain samples.
Where Was This Sold?
This product was distributed to 30 states: AZ, CA, CO, CT, DE, FL, GA, IL, IN, IA, KS, KY, MD, MA, MI, MN, MS, MO, NJ, NY, NC, OH, OK, OR, PA, SC, TX, VA, WV, DC
About Bard Peripheral Vascular Inc
Bard Peripheral Vascular Inc has 136 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report