The Recall Desk
ModerateFDA (Devices)·Z-1943-2021·Announced 2021-06-30

LED therapy device pads recalled for improper cord assembly and power failure risk

Inlightened Partners LLC is recalling 926 inLight Medical LED Pads due to improper assembly of cord connectors, which may cause power interruptions and controller shutdown.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: This is a Class III medical device recall with no reported illnesses or injuries. The hazard is a functional assembly defect in the cord connector that could cause unintended power interruption. Per the rubric, Class III recalls are typically scored 1 or 2; this voluntary precautionary recall qualifies as Moderate because the assembly defect is a functional issue rather than merely cosmetic.

Plain-English summary

Inlightened Partners LLC is recalling inLight Medical LED Pads used with Polychromatic light technology systems. The recall affects 926 units with cord connectors containing v-shaped notches that may not have been properly assembled.

The assembly defect at the cord connector could lead to power interruption, causing the controller and power supply to shut down unexpectedly.

The affected devices were distributed nationwide across the United States and Canada.

The recalled product

Product
inLight Medical LED Pads used with Polychromatic light technology system
Manufacturer
Inlightened Partners LLC
Category
Medical Device — Light therapy device
Hazard
  • power-failure
  • assembly-defect

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • All serial numbers with cord connectors that have v-shaped notches

Distribution

Distributed nationwide across the United States.

Related recalls

Same category