Medical device recalls Moderate risk

Bard Peripheral Vascular Inc recalls EnCor Breast Biopsy Probes, packaged individually in sterile pouches, 5 pouches/carton, single use, Rx, catalog/REF num…

Recall date
May 2, 2019
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2210-2019
FDA classification
Class II
Brand / firm
Bard Peripheral Vascular Inc
Sold / distributed
Worldwide distribution - US Nationwide distribution, including Puerto Rico. There was government and foreign distribution and no military distribution. Foreign distribution was made to Canada, Algeria, Australia, Austria, Belgium, Chile, China, Colombia, Croatia, Cyprus, Czech Republic, Denmark, Eg…

Why it was recalled

There has been an increase in complaints related to leaks, suction issues, and failure to obtain samples while using the product.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

EnCor Breast Biopsy Probes, packaged individually in sterile pouches, 5 pouches/carton, single use, Rx, catalog/REF numbers 10GV Upright (Vertical) - REF ECP0110GV. Product Usage: Indicated for use in acquiring tissue for diagnosing breast abnormalities.

Get recall alerts

Free email alert whenever Bard Peripheral Vascular Inc has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Bard Peripheral Vascular Inc