fda
1 records
FDA Recall: Harrow Eye LLC — Class II
20260429
Lack of Assurance of Sterility | Product: FRESHKOTE LUBRICANT EYEDROPS, Sterile, 0.33 FL OZ (10mL), Harrow Eye LLC, Nashville, TN USA.
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fda_adverse
1 records
FDA AE Manufacturer: Harrow Eye, LLC
Drug adverse event reporter — Product: DEXAMETHASONE
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