# FDA recall Z-1943-2021

> **Inlightened Partners LLC** · Class III · device recall initiated 2019-06-04.

## Product

inLight Medical LED Pads used with Polychromatic light technology system

## Reason for recall

LED pads with cord connectors that have v-shaped notches may not have been assembled properly. This issue could lead to a power interruption, causing the controller and power supply to shut down.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of CA, TX, NC, ID, CO, VA, FL, VT, AK, DC, MA, IL, AZ, MN, IA, TN, WI, WA, OK, MI, OH, GA, NY, IN, PA, NV, NJ, AR, CO , LA, MT, OR, SD, ND, MD, UT, MO, KY, NM, KS, AS, NE, WY, PR, MS and the country of Canada.

## Key facts

- **Recall number:** Z-1943-2021
- **Recalling firm:** Inlightened Partners LLC
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-06-04
- **Report date:** 2021-06-30
- **Termination date:** 2021-06-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Addison, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1943-2021

## Citation

> AI Analytics. FDA recall Z-1943-2021. Retrieved 2026-09-11 from https://api.ai-analytics.org/recall/Z-1943-2021. Source: US FDA. Licensed CC0.

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