RecallRadar

FDA Device recall Z-1177-2019

ProSun V3 42 Xlc(160w)(10 minutes) tanning bed, Model 500

On 2019-04-24 the FDA classified a Class II recall of ProSun V3 42 Xlc(160w)(10 minutes) tanning bed, Model 500 by Prosun International, citing proSun International LLC discovered discrepancies in their Quality Control Checklist documentation, which could result in high UV output.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1177-2019
ClassificationClass II
Statusterminated
Initiated2018-12-10
Published2019-04-24
Last updated2026-09-13 11:55 UTC
CompanyProsun International
DistributionUS

Product

ProSun V3 42 Xlc(160w)(10 minutes) tanning bed, Model 500. Labeled as the following: PROSUN V3 42 HIGH INTENSIVE (160W) PEARL WHITE (TMAX READY), PROSUN V3 42 HIGH INTENSIVE (160W) PEARL WHITE, PROSUN V3 42 HIGH INTENSIVE (160W) RED, PROSUN V3 42 HIGH INTENSIVE (160W) PEARL WHITE TMAX READY

Reason

ProSun International LLC discovered discrepancies in their Quality Control Checklist documentation, which could result in high UV output.

Identifiers

code_info
Serial Numbers: UN42R2AHV3C2X0111, UN42HV3C2X0435, UN42HV3C3X0450, UN42HV3C1X0414, UN42HV3C1X0407, UN42HV3C1X0410, UN42…Serial Numbers: UN42R2AHV3C2X0111, UN42HV3C2X0435, UN42HV3C3X0450, UN42HV3C1X0414, UN42HV3C1X0407, UN42HV3C1X0410, UN42HV3C1X0409, UN42HV3C3X0431, UN42HV3C2X0430

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1177-2019%22

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