Lumitex Inc: Giraffe Blue Spot PT LiteTM Phototherapy System, Model Numbers M1224917, M1231533, M1225025, M1224961, M1224958, M1224957, M1224959, M1224963, M1225773, M1225066, M1224960, M1225059, M1225023, M1225060, M1225063, M1225064, M1225024, M1231622, M1236303, M1238489, M1238490, M1238492, M1238493, M1238495, M1238499, M1238503, M1238505, M1238507, M1238508, 2063860-001, 2063862-001, 2063870-001, 2063873-001, 2063874-001, 2071393-001, 2080916-001, 2089424-001

Recall number

Z-0923-2020

Recalling firm

Lumitex Inc

Product

Giraffe Blue Spot PT LiteTM Phototherapy System, Model Numbers M1224917, M1231533, M1225025, M1224961, M1224958, M1224957, M1224959, M1224963, M1225773, M1225066, M1224960, M1225059, M1225023, M1225060, M1225063, M1225064, M1225024, M1231622, M1236303, M1238489, M1238490, M1238492, M1238493, M1238495, M1238499, M1238503, M1238505, M1238507, M1238508, 2063860-001, 2063862-001, 2063870-001, 2063873-001, 2063874-001, 2071393-001, 2080916-001, 2089424-001

Status

Terminated

Initiated

2019-12-11

Posted

not on file

Terminated

2021-09-08

Reason

There is a potential for some systems built between 2014 and Jan 2018 to have a light output falling below the recommended minimum output. This problem has been associated with exposure of the light pipe to elevated temperatures, which is contra-indicated in the Operation, Maintenance, and Service Manual.

Root cause

Device Design

Action

An Urgent Medical Device Correction notification letter was sent to the customer. Actions to be taken by the Customer/User: Please notify all end users, that have received the above listed product that to ensure the patient gets proper levels of treatment they should take the following actions. 1. Immediately check all your device outputs using a BiliBlanket Meter II bilimeter and continue to do so prior to every use, as listed in the Instructions for Use as well as during the treatment session. Instructions as to how to measure your devices output are provided in both the Operation, Maintenance, and Service Manual Section 2.1 Pre-Use Checkout Procedure and in the Quick Reference Guide attached to every unit and are detailed below in Appendix 1. Take out of service any units found to have irradiance levels less than 27W/cm2/nm and await the free kit to correct the unit that GE Healthcare will be sending for all potentially affected units. Elevated heat can cause the light pipe optical fiber to protrude through its reflector aperture, creating an unfocused spot with less than 27W/cm2/nm output as described above. The photos below show the effect and can be used in conjunction with the BiliBlanket Meter II bilimeter to identify units with a low light condition due to elevated heat exposure. 2. As previously stated, exposing the shade head to elevated heat from the warmer is contra-indicated with this device. To prevent potential damage to light pipes due to elevated heat, we remind that care should be taken to position the light pipe, as shown in the Instructions for Use Section 2.2 Operation and in the Quick Reference Guide, keeping the light pipe Shade head outside the direct path of warmers. Product Correction: To correct any existing devices experiencing low light output due to fiber protrusion and to prevent potential future low light output due to fiber protrusion, GE Healthcare will send a kit to fix all potentially affected units free of c

Quantity

6837

Distribution

The products were distributed to the following US states: WI.

Lot, serial or model codes

2014 Production Serial Numbers: All Serial numbers beginning with QAAT;  2015 Production Serial Numbers: All Serial numbers beginning with QAAU;  2016 Production Serial Numbers: All Serial numbers beginning with QAAV;  2017 Production Serial Numbers: All Serial numbers beginning with QAAW;  2018 Production Serial Numbers: Serial numbers QAAT60001 through QAAT60156

510(k) numbers

["K120820"]

PMA numbers

not on file

Product code

LBI

Firm FEI

1000122810

Firm city

Strongsville

Firm state

OH

Firm country

not on file

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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