CIVCO Biopsy Starter Kit recall: Sterility Concern

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

M475840, M475850, M483080, M184760, M201120, M201220, M201230, M229890, M230450, M248410, M265470, M282270, M307490, M322230, M367370, M370090, M381360, M421260, M431550, M452150, M458370, M488300, M514070, M572510, M576810, M606320, M626250, M639290, M642350, M648020, M540640, M543800, M551990, M592190, M604120, M448100, M477600, M477700, M504340, M504350, M507520, M524270, M544100, M569330, M569340, M590710, M600460, M632390, M643140, M604180, M091360, M109060, M122250, M186540, M202260, M253050, M275630, M308820, M335740, M425050, M457560, M483250, M499390, M547370, M559550, M118570, M206960, M425030, M430820, M085360, M089740, M099100, M107610, M118700, M137600, M201810, M220800, M231940, M353380, M358810, M394960, M425020, M430810, M448670, M476410, M488580, M497660, M547740, M598410, M632210, M633570, M085370, M118680, M155510, M173420, M187860, M205340, M353390, M358170, M358580, M358590, M391700, M391710, M395610, M430800, M451470, M616810, M654380, M118610, M451460, M118650, M139440, M141830, M225010, M338400, M435250, M448680, M463740, M499630, M623350, M119380, M206950, M358560, M358570, M381520, M427660, M440600, M526290, M526300, M118660, M141820, M190870, M272570, M435240, M491500, M508640, M622060, M106080, M118600, M124610, M148440, M268900, M283940, M317630, M358610, M381510, M391680, M484430, M484440, M492320, M526260, M526270, M118710, M148450, M490000, M593130, M162020, M205920, M317680, M210700, M262520, M297390, M317690, M334110, M347120, M369110, M373250, M379350, M385180, M390160, M450210, M500620, M539310, M541330, M541830, M448110, M448120, M460670, M472720, M524230, M534750, M536730, M557450, M566960, M593280, M598060, M627710, M552010, M455790, M480870, M510000, M541140, M541810, M576640, M600450, M609740, M610550, M636940, M643130, M650780, M085390, M120660, M177390, M295660, M352830, M355940, M395670, M408960, M430430, M463720, M530670, M568980, M609970, M620480, M663970, M056500, M096880, M112390, M119730, M232970, M251160, M261840, M304420, M374360, M419670, M440460, M475460, M497670, M545750, M603800, M085550, M089260, M093020, M103030, M105150, M183050, M220960, M293580, M293590, M388690, M419650, M560740, M056760, M103040, M124110, M183060, M234590, M312170, M436670, M436680, M444740, M598550, M639430, M093010, M119280, M120400, M120860, M142690, M158480, M220970, M237740, M242000, M261770, M388700, M407620, M419660, M444950, M598860, M328300, M330340, M345110, M349600, M381530, M464980, M547940, M598070, M624410, M117130, M139400, M142090, M164840, M186690, M190180, M193400, M201660, M205110, M232930, M234630, M275650, M297260, M322700, M327850, M335060, M368160, M423720, M430440, M435750, M456910, M475140, M477930, M504290, M528270, M570840, M576930, M639440, M088430, M089650, M091400, M095990, M102210, M116290, M119930, M124320, M133350, M134540, M135520, M139740, M144670, M163200, M163260, M171240, M179410, M187920, M192750, M202990, M213370, M217330, M223270, M229780, M231960, M245390, M253360, M280960, M299320, M346870, M382670, M394080, M394090, M397380, M423700, M437090, M476650, M542430, M544290, M573360, and M618690

Product

CIVCO Biopsy Starter Kit, Reusable non-sterile bracket with Infiniti Plus (12, 14, 16, 18GA) needle guides, Rx ONLY. REFs 10787043, 11001906…

Recalling firm

Civco Medical Instruments Co. Inc.

Quantity

1139 boxes

Distribution

Worldwide Distribution - US (nationwide) and Internationally to AUSTRALIA, AUSTRIA, BELGIUM, CANADA, CHILE, CHINA (MAINLAND), CHINA (TAIWAN), CZECH REPUBLIC, DENMARK, ECUADOR, FINLAND, FRANCE, GERMANY, HONG KONG, INDIA, ISRAEL, ITALY, JAPAN, KUWAIT, NETHERLANDS, NEW ZEALAND, NORWAY, POLAND, PUERTO RICO, QATAR, SOUTH AFRICA, ROMANIA, SAUDI ARABIA, SINGAPORE, SOUTH KOREA, SPAIN, SWITZERLAND, TRINIDAD AND TOBAGO, TURKEY, UGANDA, UKRAINE, and UNITED KINGDOM.

Recall date

November 25, 2015

Classification

Class II

Status

Terminated

Agency

FDA (device)