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MedWatch Adverse Event Reporting

Massive New Nationwide Recall Issued For 27 Eye Drop Products Due To 'Insanitary Conditions' Massive New Nationwide Recall Issued For 27 Eye Drop Products Due To 'Insanitary Conditions'
Massive New Nationwide Recall Issued For 27 Eye Drop Products Due To 'Insanitary Conditions' A new nationwide recall has been issued for 27 eye drop products. The drops, distributed to wholesalers and retailers by Velocity Pharma LLC,  are being recalled due to potential safety concerns after Food and Drug Administration (FDA) investigators found insanitary conditions. All lots subject to the recall have expiration dates ranging from November 2023 to September 2025. For a table listing all 27 brands involved, click this link from the FDA. A risk statement accompanying the recall says: "For those patients who use these products, there is a potential risk of eye infections or…
Recall Issued For Supplement Due To Presence Of Undeclared Ingredient Recall Issued For Supplement Due To Presence Of Undeclared Ingredient
Recall Issued For Supplement Due To Presence Of Undeclared Ingredient A company recalled a supplement that was sold across the United States due to the presence of an undeclared ingredient.  Distributor RFR LLC recalled SANGTER Energy Supplements 3000mg with expiration date 01/2025 after Food & Drug Administration analysis found the products contained undeclared sildenafil, a substance found in FDA-approved treatments of male erectile dysfunction, according to an FDA announcement on Tuesday, Aug. 2. The presence of sildenafil makes the supplements an unapproved new drug, the FDA reported.  Undeclared sildenafil can interact with nitrates f…