Recall: Lubrisine Eye Drops
On 2018-12-31, the FDA announced that Results RNA is conducting a recall on Eye Drops due to a possible lack of sterility. The recalled products were sold under the brand name(s) Lubrisine during an unspecified time period throughout the regions shown in the map below.
In recent months, there have been 2 drugs recalls due to potential lack of sterility, including eye relief drops, 0.5 oz. (15ml) bottle, sterile compounded drugs and more. Additionally, there have been 18 drug and medical device recalls due to other health hazards as well as 95 food recalls.
Company Contact Information:
Name: Results RNA
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Detailed Recall Information
Regions Where Sold: Because the region was not specified, it is assumed that this product was available nationwide.
Product Description: Eye Drops
Brand Name(s): Lubrisine
Reason for Recall: Undeclared colloidal silver and lack of sterility assurance
Official Recall Date: 2018-12-31
Additional information provided by the FDA.gov:
Results RNA LLC is voluntarily recalling Lubrisine Eye Drops to the healthcare practitioner, retail or consumer level. This product, in a recent FDA inspection, was found to be manufactured using practices that do not support its sterility and contained undeclared colloidal silver. Read More.
More information may be available at FDA.gov
Latest Safety Recalls
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Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.