Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LDI Laser firmware lower than V02.13.00 for LDI models: LDl-7 Recalled by 89 NORTH Due to The defect relates to firmware version lower than...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact 89 NORTH directly.
Affected Products
LDI Laser firmware lower than V02.13.00 for LDI models: LDl-7, LDI-WF, LDI-NIR, LDl-6 Laser Science fluorescence imaging
Quantity: 188
Why Was This Recalled?
The defect relates to firmware version lower than V02.13.00. It is controlling safety interlocks of the LDI; specifically, the potential for the LDI to enter a service mode intended for use in the factory environment only which overrides all interlocks. When this mode - "Interlock Override Mode" - is entered, the system does not cease laser emission when interlocks are opened, but rather allows emission to continue with open interlocks. The potential for this to occur is non-compliant with 21CFR 1040 .10{f )(2) and 21 CFR 1040 .10(f)(3).
Where Was This Sold?
Worldwide
About 89 NORTH
89 NORTH has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report