Dermalight 80 recall
Dermalight 80 Model Number UVB-083, one unit per box. The Dermalight 80 is a Phototherapy light unit that provides ultraviolet radiation therapy for…
Why was Dermalight 80 recalled?
The incorrect manual may have been packaged with this product. UVB-083 devices may have included the manual for a UVA-080 device.
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?
The following batch and serial numbers are affected by the recall: Batch 007778, Serial numbers D83-30016 to D83-30021.
- Product
- Dermalight 80 Model Number UVB-083, one unit per box. The Dermalight 80 is a Phototherapy light unit that provides ultraviolet radiation therapy for…
- Recalling firm
- National Biological Corp
- Quantity
- 6 units
- Distribution
- US distribution including the states of: AL, CA, MN, and NC.
- Recall date
- July 31, 2013
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)