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U.S. Department of Health and Human Services

Class 2 Device Recall Sundream 12 V tanning bed

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 Class 2 Device Recall Sundream 12 V tanning bedsee related information
Date Initiated by FirmDecember 02, 2017
Create DateJanuary 05, 2018
Recall Status1 Terminated 3 on February 18, 2026
Recall NumberZ-0319-2018
Recall Event ID 78571
Product Classification Booth, sun tan - Product Code LEJ
ProductSundream 12 V tanning bed
Code Information 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
FEI Number 1000525872
Recalling Firm/
Manufacturer		 ProSun International, LLC
2442 23rd St N
Saint Petersburg FL 33713-4018
For Additional Information ContactJennifer Camison Henkemans
727-825-0400
Manufacturer Reason
for Recall		The 30 minute maximum tanning time has been reduced to 20 minutes.
FDA Determined
Cause 2		Other
ActionCustomers 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 Commerce75 units
DistributionDistributed 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
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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