Sundream 12 V tanning bed recall
Sundream 12 V tanning bed
Why was Sundream 12 V tanning bed recalled?
The 30 minute maximum tanning time has been reduced to 20 minutes.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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
- Product
- Sundream 12 V tanning bed
- Recalling firm
- ProSun International, LLC
- Quantity
- 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
- Recall date
- January 17, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)