FDA Device recall Z-0282-2023
VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam Combiner) Product Number: 161-0001
- FDA Device
- Class II
- ongoing
- Published 2022-11-30
On 2022-11-30 the FDA classified a Class II recall of VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam Combiner) Product Number: 161-0001 by Visionsense, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0282-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-10-17 |
| Published | 2022-11-30 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Visionsense |
| Distribution | US |
Product
VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam Combiner) Product Number: 161-0001
Reason
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.
Identifiers
| code_info | UDI-DI: 18130400103625 Lot Numbers: Serial Number/Lot Number 3611111 3611161 3611191 361-0012 361-0901 361-0902 361-090…UDI-DI: 18130400103625 Lot Numbers: Serial Number/Lot Number 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 3610975 3610977 3610978 3610979 3610996 3610998 3610999 3611000 3611004 3611006 3611007 3611008 3611009 3611011 3611012 3611014 3611015 3611016 3611019 3611025 3611027 3611029 3611031 3611033 3611034 3611035 3611036 3611039 3611041 3611042 3611044 3611046 3611048 3611049 3611052 3611053 3611055 3611056 3611057 3611058 3611059 3611060 361-1061 3611062 3611063 3611065 361-1067 3611068 3611070 3611071 3611073 3611075 3611 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0282-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.