RecallRadar

FDA Device recall Z-2209-2019

EnCor Breast Biopsy Probes, packaged individually in sterile pouches, 5 pouches/carton, single use, Rx, catalog/REF number 10G - REF ECP011…

On 2019-08-14 the FDA classified a Class II recall of EnCor Breast Biopsy Probes, packaged individually in sterile pouches, 5 pouches/carton, single use, Rx, catalog/REF number 10G - REF ECP011… by Bard Peripheral Vascular, citing there has been an increase in complaints related to leaks, suction issues, and failure to obtain samples while using the product.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2209-2019
ClassificationClass II
Statusterminated
Initiated2019-05-02
Published2019-08-14
Last updated2026-09-13 11:55 UTC
CompanyBard Peripheral Vascular
DistributionUS

Product

EnCor Breast Biopsy Probes, packaged individually in sterile pouches, 5 pouches/carton, single use, Rx, catalog/REF number 10G - REF ECP0110G. Product Usage: Indicated for use in acquiring tissue for diagnosing breast abnormalities.

Reason

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

Identifiers

code_info
Lot numbers VTCT0306, VTCT0307, VTCU0358 VTCU0359, VTCU0360, VTCU0361, VTCV0369, VTCW0454, VTCW0455, VTCW0456, VTCW0479…Lot numbers VTCT0306, VTCT0307, VTCU0358 VTCU0359, VTCU0360, VTCU0361, VTCV0369, VTCW0454, VTCW0455, VTCW0456, VTCW0479, VTCX0482, VTCX0483, VTCX0484, VTCY0536, VTCY0544, VTCY0545, VTCY0546, VTCY0547, VTCZ0637, VTCZ0638, VTCZ0639, VTCZ0641, VTCZ0647, VTDN0035, and VTDN0036.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2209-2019%22

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