Z-0319-2018Class II

Sundream 12 V tanning bed

Name: Z-0319-2018 Sundream 12 V tanning bed
Creator: ProSun International, LLC
Published: 2017-12-02
License: https://open.fda.gov/license/

J&T Health and Wellness LLC / initiated 2017-12-02 / Terminated

FDA source

ProSun International, LLC began a recall of Sundream 12 V tanning bed on 2017-12-02. FDA classified it as Class II and gives the reason as "The 30 minute maximum tanning time has been reduced to 20 minutes". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0319-2018
Classification: Class II
Status: Terminated
Initiated: 2017-12-02
Posted: 2018-01-05
Terminated: 2026-02-18
Recalling firm: J&T Health and Wellness LLC
Product: Sundream 12 V tanning bed
Product code: LEJ Booth, Sun Tan
Reason for recall: The 30 minute maximum tanning time has been reduced to 20 minutes.
FDA root cause: Other
Action: Customers were initially notified of the recall on 03/24/2016 and then again on 10/17/2017. Instructions included to check current inventory for the affected device and complete and return the response card to ProSun who will then supply a set of 12 lower output lamps that are rated at 30 minutes maximum tanning time, provide a new Owner's Manual, and a new Tanning Schedule Label with the new 30 min lamps listed.
Quantity in commerce: 75 units
Distribution: Distributed domestically to AK, AL, AZ, CA, CT, FL, GA, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NH, NV, NY, OH, OK, PA, SC, TN, TX, UT, WA, WI
Product codes and lots: Model No. 12V, Serial No. SUN12VH1R0006, SUN12VH1R0005, SUN12VH1R0001, SUN12VH1R0004, SUN12VH1R0002, SUN12VH1R0003, SUN12VH1R0007, SUN12VH1R1001, SUN12VH1R0011, SUN12VH1R0012, SUN12VH1R0013, SUN12VH1R0009, SUN12VH1R0010, SUN12VH1R0016, SUN12VH1R0015, SUN12VH1R0017, SUN12VH1R0018, SUN12VH1R0022, SUN12VH1R0021, SUN12VH1R0019, SUN12VH1R0020, SUN12VH1R0023, SUN12VH1R0024, SUN12VH1R0026, SUN12VH1R0027, SUN12VH1R0025, SUN12VH1R0028, SUN12VH1R0033, SUN12VH1R0036, SUN12VH1R0039, SUN12VH1R0041, SUN12VH1R0042, SUN12VH1R0047, SUN12VH1R0043, SUN12VH1R0045, SUN12VH2R0032, SUN12VH1R0040, SUN12VH1R0031, SUN12VH1R0044, SUN12VH1R0050, SUN12VH1R0049, SUN12VH1R0048, SUN12VH1R0055, SUN12VH1R0056, SUN12VH1R0054, SUN12VH1R0057, SUN12VH1S0060, SUN12VH1S0059, SUN12VH1S0058, SUN12VH1R0052, SUN12VH1S0061, SUN12VH1S0062, SUN12VH1R0051, SUN12VH4R0053, SUN12VH1S0063, SUN12VH1S0066, SUN12VH1S0064, SUN12VH1S0065, SUN12VH1S0071, SUN12VH1S0070, SUN12VH1S0068, SUN12VH1S0073, SUN12VH1R0072, SUN12VH1S0075, SUN12VH1S0067, SUN12VH1S0076, SUN12VH1S0069, SUN12VH1S0074, SUN12VH1S0077, SUN12VH1S0079, SUN12VH2S0080, SUN12VH1S0086, SUN12VH2S0081, SUN12VH1R0087, SUN12VH1R0088

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0319-2018
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0319-2018	Class II	Terminated	Voluntary: Firm initiated	2018-01-17	2018-01-05

Product code LEJ

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)