inLight Medical LED Pads with v-shaped notch cord connectors may cause power shutdowns. Recalled due to improper assembly risk of interruption.
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.
Inlightened Partners is recalling LED pads used with Polych: light systems because improper assembly of cord connectors with v-shaped notches could cause power interruptions. This may lead to the controller and power supply shutting down unexpectedly.
The v-shaped notches in cord connectors may not have been assembled correctly. This can cause power interruptions, leading to the controller and power supply shutting down unexpectedly.
Users of inLight Medical LED Pads with cord connectors featuring v-shaped notches are affected. Those using these pads with Polychromatic light systems are most at risk.
Check for v-shaped notches on the cord connectors of inLight Medical LED Pads. The recall covers all units with this specific connector design used with Polychromatic light technology systems.
Inspect cord connectors for v-shaped notches to determine if the product is recalled.
The recall is due to improper assembly of cord connectors with v-shaped notches, which could cause power interruptions and shutdowns of the controller and power supply.
Check for v-shaped notches on the cord connectors of inLight Medical LED Pads used with Polychromatic light technology systems.
The recall does not specify a remedy, so check with the manufacturer for further instructions.
We’ve drafted a message you can send Inlightened Partners to request your refund or repair — edit it as you like.
Subject: Recall Z-1943-2021 — Inlightened Partners Inlightened Partners Hello, I own a Inlightened Partners that is covered by recall Z-1943-2021 from Inlightened Partners. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
