The product does not meet the requirements of the General Product Safety Regulations 2005. If you have this product and think it may be one of the affected batches do not use it. If you are not sure if you have an affected product, you can send photos of the bottle including the batch number on the bottom of the bottle to: sinusrecall@detoxpeople.eu
Below is information on the affected batches listing the order number and then the lot number: 518151 - 2108021HFA 518150 - 2108021HFA 480659 - 210726SS01 480657 - 210726SS01 443688 - 210726SS01 378470 - 210303SS01 326462 - 201009SS01 293015 - 200724SS011 283545 - 200430SS011 276321 - 200430SS011 276296 - 200430SS011 262086 - 200402SS011FC 255069 - 200311SS11-GM Sales period: June 2017 to September 2019
The product has been identified as presenting a microbiological risk as testing found the product to contain microbial contamination identified as Microbacterium sp, Fictibacillus sp, Bacillus sp, (primarily B. malikii), and Paenibacillus sp.
The use of the affected product could potentially result in severe or life-threatening adverse events such as bacteremia or fungemia, invasive bacterial or fungal rhinosinusitis, or disseminated fungal infection.
For more information see attached Recall Notice.
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