FDA Device recall Z-1943-2021
inLight Medical LED Pads used with Polychromatic light technology system
- FDA Device
- Class III
- terminated
- Published 2021-06-30
On 2021-06-30 the FDA classified a Class III recall of inLight Medical LED Pads used with Polychromatic light technology system by Inlightened Partners, citing 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 supp….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1943-2021 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2019-06-04 |
| Published | 2021-06-30 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Inlightened Partners |
| Distribution | US |
Product
inLight Medical LED Pads used with Polychromatic light technology system
Reason
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.
Identifiers
| code_info | All serial numbers with cord connectors that have v-shaped notches |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1943-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.