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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 73779

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
March 30, 2016
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
LED Technologies, LLC

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

reVive Light Therapy Pain Relief Device (Model Number: RVPNSYS) Product Usage: The reVive Light Therapy Pain Relief Device is a device designed to deliver LED light spectrum in 880nm and 660nm directly into the body tissue to increase circulation and temporarily relieve pain associated with muscle spasms, arthritis, general aches and strains.

Z-1581-2016
Recall number
Z-1581-2016
Initiated
March 30, 2016
Classification
Class II
Status
Terminated
Recalling firm
LED Technologies, LLC
Quantity
32 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Incorrect Power Supply in the package, rendering the device inoperable.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrect Power Supply in the package, rendering the device inoperable.

Code information

Manufactured between 12/15/2015 and 12/28/2015 for specific lot #1052

Distribution pattern

Distributed to 1 consignee located in the United States.