Reported Nov 30, 2022 · Ongoing

VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam Combiner) Product Number: 161-0001

Visionsense, Ltd.

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: Visionsense, Ltd. · 20, Ha-Magshimim · Petakh Tikva, N/A · N/A

Is this the product you have?

  • VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam
  • Combiner) Product Number161-0001
Lot codes and dates
  • UDI-DI18130400103625
  • Lot NumbersSerial Number/Lot Number

    204 of 204 codes

    • 3611111
    • 3611161
    • 3611191
    • 361-0012
    • 361-0901
    • 361-0902
    • 361-0903
    • 361-0904
    • 361-0906
    • 361-0907
    • 361-0908
    • 361-0909
    • 361-0910
    • 361-0911
    • 361-0913
    • 361-0914
    • 361-0915
    • 361-0916
    • 361-0917
    • 361-0918
    • 361-0919
    • 361-0921
    • 361-0922
    • 361-0923
    • 361-0924
    • 361-0926
    • 361-0929
    • 361-0931
    • 361-0932
    • 361-0933
    • 361-0937
    • 361-0938
    • 361-0940
    • 361-0941
    • 3610942
    • 361-0943
    • 361-0944
    • 361-0945
    • 3610946
    • 3610947
    • 3610949
    • 3610950
    • 3610951
    • 3610952
    • 3610953
    • 361-0955
    • 3610956
    • 3610957
    • 3610958
    • 3610961
    • 3610963
    • 3610964
    • 3610965
    • 361-0966
    • 3610968
    • 361-0970
    • 3610971
    • 3610972
    • 3610973
    • 3610974
Amount recalled
204 units: 93 units OUS ; 111 units US

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

Broken Optical fiber cable damage can occur through handling or bending and can lead to loss of functionality and heating/melting of the outer cable surface.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:53 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.