Biocare Systems Inc. LumiWave 1X4 Infrared Therapy Device, Catalog # LW1X4, BioCare Systems, Inc. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
LumiWave 1X4 Infrared Therapy Device, Catalog # LW1X4, BioCare Systems, Inc.
Brand
Biocare Systems Inc.
Lot Codes / Batch Numbers
Catalog # LW1X4, all units, all lots
Products Sold
Catalog # LW1X4, all units, all lots
Biocare Systems Inc. is recalling LumiWave 1X4 Infrared Therapy Device, Catalog # LW1X4, BioCare Systems, Inc. due to Electrical Safety Hazard-when pulling on the cord of the AC adapter, to remove it from an outlet, the prongs on the AC adapter, may detach from the u. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Electrical Safety Hazard-when pulling on the cord of the AC adapter, to remove it from an outlet, the prongs on the AC adapter, may detach from the unit, damaging it and exposing the user to an electrical safety hazard
Recommended Action
Per FDA guidance
Consignees were notified by telephone beginning 06/08/2006, followed by a letter on 06/23/2006.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026