Reported Oct 7, 2015 · Terminated

EVIS EXERA II Gastrovideoscope OLYMPUS GF type UCT180; designed for endoscopic real-time ultrasound imaging, ultrasound…

Olympus Corporation of the Americas

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Olympus Corporation of the Americas · PO Box 610 · Center Valley, PA · 18034-8229

Is this the product you have?

  • EVIS EXERA II Gastrovideoscope OLYMPUS GF type UCT180; designed for endoscopic real-time ultrasound imaging, ultrasound guided needle aspiration and other endoscopic procedures within the upper gastrointestinal tract and surrounding organs.
Lot codes and dates
  • ModelsGF-UCT180
  • with serial numbers

    1,039 of 1,039 codes

    • 1110499
    • 1210800
    • 7410282
    • 1310997
    • 1311003
    • 1311004
    • 1310999
    • 1311000
    • 1210572
    • 7310007
    • 7310012
    • 1210883
    • 1310886
    • 7510736
    • 7510753
    • 1110488
    • 1110309
    • 7410481
    • 7410477
    • 7310025
    • 7510647
    • 7510648
    • 7510811
    • 7510810
    • 7510809
    • 7510832
    • 7510830
    • 7510827
    • 7510704
    • 7410530
    • 7410524
    • 7410526
    • 7410525
    • 7510734
    • 7510726
    • 7510688
    • 1210542
    • 7410289
    • 1311015
    • 1311016
    • 7410335
    • 1210874
    • 7410426
    • 1210687
    • 7410546
    • 7410145
    • 7310031
    • 1110477
    • 1110479
    • 1110497
    • 1310945
    • 1110511
    • 1110482
    • 7510569
    • 7410353
    • 1110397
    • 1100203
    • 1100198
    • 1110457
    • 1110504
Amount recalled
1014

Where it was sold

  • Nationwide

Why it was recalled

Insufficient information for specific cleaning accessories used for the cleaning and reprocessing of the GF-UCT180 ultrasound endoscope

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated May 8, 2017 · Data as of Sep 19, 5:25 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.