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FDA Safety Information on Drugs & Medical Devices

May 8, 2017Newsgaladmin

Natural Dior LLC Issues Voluntary Nationwide Recall of Vitafer-L Gold Liquid Due to Presence of Undeclared Tadalafil
Source: FDA MedWatch Safety Alert Published on 2025-02-26 By FDA
Central Admixture Pharmacy Services (CAPS) Issues Nationwide Recall of Phenylephrine 40 mg Added to 0.9% Sodium Chloride 250 mL in 250 mL Excel Bags Due to Visible Black Particulate Matter in a Single-Sealed Vial
Source: FDA MedWatch Safety Alert Published on 2025-02-25 By FDA
Ascent Consumer Products Inc. Issues Voluntary Nationwide Recall of SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System Due to Microbial Contamination
Source: FDA MedWatch Safety Alert Published on 2025-02-25 By FDA
FDA 101: How to Use the Consumer Complaint System and MedWatch
Source: FDA Consumer Health Information Updates Published on 2025-02-24 By FDA
Avoid Dangerous HCG Diet Products
Source: FDA Consumer Health Information Updates Published on 2025-02-24 By FDA
Pacemaker Recall: Boston Scientific Corporation Recalls Accolade Pacemaker Devices Due to a Manufacturing Issue That May Lead to Early Device Replacement
Source: FDA MedWatch Safety Alert Published on 2025-02-21 By FDA
One Source Nutrition, Inc. Issues Voluntary Nationwide Recall of Vitality Capsules Due to Presence of Undeclared Sildenafil and Tadalaﬁl
Source: FDA MedWatch Safety Alert Published on 2025-02-20 By FDA
BD Announces Voluntary Worldwide Recall for One Lot of ChloraPrep™ Clear 1 mL Applicators Due to Fungal Contamination
Source: FDA MedWatch Safety Alert Published on 2025-02-18 By FDA
Heart Pump Recall: Abiomed, Inc. Updates Use Instructions for Impella RP with SmartAssist and Impella RP Flex with SmartAssist Due to A Risk That the Tip of Guidewires or Other Medical Devices May Come into Contact with The Impella Pump During Insertion, Adjustment, Or Removal
Source: FDA MedWatch Safety Alert Published on 2025-02-14 By FDA
ICU Medical Issues Nationwide Recall of Potassium Chloride Injection, 20 mEq and Potassium Chloride Injection, 10 mEq Due to Mislabeling
Source: FDA MedWatch Safety Alert Published on 2025-02-14 By FDA
VITALITY may be harmful due to hidden drug ingredients
Source: FDA - Tainted Products That are Marketed as Dietary Supplements RSS Feed Published on 2025-02-10 By FDA
bio LIT may be harmful due to hidden drug ingredient
Source: FDA - Tainted Products That are Marketed as Dietary Supplements RSS Feed Published on 2025-02-10 By FDA
vROX may be harmful due to hidden drug ingredient
Source: FDA - Tainted Products That are Marketed as Dietary Supplements RSS Feed Published on 2025-02-10 By FDA
ADVANCE KING may be harmful due to hidden drug ingredients
Source: FDA - Tainted Products That are Marketed as Dietary Supplements RSS Feed Published on 2025-02-10 By FDA
HimGo may be harmful due to hidden drug ingredients
Source: FDA - Tainted Products That are Marketed as Dietary Supplements RSS Feed Published on 2025-02-10 By FDA

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