Drugs.com - FDA MedWatch Alerts

CAPS Issues 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

CAPS Issues Recall of Phenylephrine 40 mg Added to 0.9%...

Feb 26, 2025 0

Audience: Pharmacy, Health Care Professional February 24, 2025 – Bethlehem, PA. ...

One Source Nutrition, Inc. Issues Voluntary Nationwide Recall of Vitality Capsules Due to Presence of Undeclared Sildenafil and Tadalaﬁl

One Source Nutrition, Inc. Issues Voluntary Nationwide ...

Feb 23, 2025 0

Audience: Consumer Benton, Arkansas – February 20, 2025 –One Source Nutrition is...

ICU Medical Issues Nationwide Recall of Potassium Chloride Injection, 20 mEq and Potassium Chloride Injection, 10 mEq Due to Mislabeling

ICU Medical Issues Nationwide Recall of Potassium Chlor...

Feb 16, 2025 0

Audience: Consumer, Health Professional, Pharmacy February 13, 2025 LAKE FOREST,...

FDA, FTC Continue Joint Effort to Protect Consumers Against Companies Illegally Selling Copycat Delta-8 THC Food Products

FDA, FTC Continue Joint Effort to Protect Consumers Aga...

Feb 9, 2025 0

Audience: Consumer July 16, 2024 -- Today, the U.S. Food and Drug Administration...

GURU INC. Issues Voluntary Nationwide Recall of Infla-650 Herbal Dietary Supplement Capsules Due to Hidden Drug Ingredients

GURU INC. Issues Voluntary Nationwide Recall of Infla-6...

Feb 9, 2025 0

Audience: Consumer Lilburn, GA, July 16, 2024 -- GURU INC. is voluntarily recall...

Endo USA, Inc. Issues Recall of One Lot of Clonazepam Orally Disintegrating Tablets Due to Mislabeling: Incorrect Strength on Product Carton

Endo USA, Inc. Issues Recall of One Lot of Clonazepam O...

Feb 9, 2025 0

Audience: Healthcare Provider, Pharmacy, Consumer MALVERN, PA, July 16, 202...

Aurobindo Pharma USA, Inc. on Behalf of AuroHealth, Issues Recall of One Lot of Healthy Living Over the Counter (OTC) Migraine Relief

Aurobindo Pharma USA, Inc. on Behalf of AuroHealth, Iss...

Feb 9, 2025 0

Audience: Healthcare Provider, Pharmacy, Consumer July 18, 2024 – East Windsor, ...

Hikma Pharmaceuticals USA Inc. Extends Voluntary Nationwide Recall of One Lot of Acetaminophen Injection, 1000mg/100mL (10mg/mL) Bags

Hikma Pharmaceuticals USA Inc. Extends Voluntary Nation...

Feb 9, 2025 0

Audience: Healthcare Provider, Pharmacy, Consumer London, July 22, 2024 – Hikma ...

Main Products, Inc. Issues Recall of Umary Acido Hialuronico, Suplemento Alimenticio Due to the Presence of Undeclared Drug Ingredients

Main Products, Inc. Issues Recall of Umary Acido Hialur...

Feb 9, 2025 0

Audience: Consumer, Health Professional, Pharmacy, Pain Management, Gastroentero...

FDA Warns Against Purchasing or Using Chemical Peel Skin Products Without Professional Supervision

FDA Warns Against Purchasing or Using Chemical Peel Ski...

Feb 9, 2025 0

Audience: Consumer July 30, 2024 -- FDA is warning consumers not to purchase or ...

Baxter Issues Voluntary Nationwide Recall of One Lot of Heparin Sodium in 0.9% Sodium Chloride Injection Due to Potential for Elevated Endotoxin Levels

Baxter Issues Voluntary Nationwide Recall of One Lot of...

Feb 9, 2025 0

Audience: Healthcare Provider, Pharmacy, Consumer DEERFIELD, Ill., AUG. 5, 2024 ...

FDA Warns Consumers to Not Purchase or Use Unapproved Inhalant Products Marketed for Alertness and Energy Boosting

FDA Warns Consumers to Not Purchase or Use Unapproved I...

Feb 9, 2025 0

Audience: Consumer August 6, 2024 -- FDA is warning consumers to not purchase or...

B. Braun Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride for Injection USP 1000 mL in E3 Containers Due to the Potential for Particulate Matter and Leakage

B. Braun Issues Voluntary Nationwide Recall of 0.9% Sod...

Feb 9, 2025 0

Audience: Healthcare Provider, Pharmacy, Consumer BETHLEHEM, PA - August 8, 2024...

Boulla LLC Issues Voluntary Nationwide Recall of Boom Max Capsules Due to the Potential Presence of Undeclared Sildenafil

Boulla LLC Issues Voluntary Nationwide Recall of Boom M...

Feb 9, 2025 0

Audience: Consumers August 14, 2024 – Sacramento CA, Boulla LLC is voluntarily r...

Veata LLC Issues Voluntary Nationwide Recall of Endurance Pro Capsules Due to the Potential Presence of Undeclared Sildenafil

Veata LLC Issues Voluntary Nationwide Recall of Enduran...

Feb 9, 2025 0

Audience: Consumers August 14, 2024 – Sacramento CA, Veata LLC is voluntarily re...

FDA Warns Consumers Not to Purchase or Use Umary and Amazy Products As They May Be Harmful To Your Health

FDA Warns Consumers Not to Purchase or Use Umary and Am...

Feb 9, 2025 0

Audience: Consumers September 5, 2024 -- FDA is warning consumers not to purchas...

Bionpharma Inc. Issues Voluntary Nationwide Recall of Atovaquone Oral Suspension Due to Bacterial Contamination

Bionpharma Inc. Issues Voluntary Nationwide Recall of A...

Feb 9, 2025 0

Audience: Healthcare Provider, Pharmacy, Consumer September 17, 2024 – Princeton...

Drug Safety Communication: FDA Adds Warning About Rare Occurrence of Serious Liver Injury with Use of Veozah (fezolinetant) for Hot Flashes Due to Menopause

Drug Safety Communication: FDA Adds Warning About Rare ...

Feb 9, 2025 0

Audience: Patient, Health Professional, OBGYN, Endocrinology September 12, 2024 ...

Gilead Issues Voluntary Nationwide Recall of One Lot of Veklury (Remdesivir) for Injection 100 mg/vial Due to the Presence of a Glass Particle

Gilead Issues Voluntary Nationwide Recall of One Lot of...

Feb 9, 2025 0

Audience: Healthcare Provider, Pharmacy Foster City, Calif., September 20, 2024 ...

Staska Pharmaceuticals, Inc. Issues Recall of Ascorbic Acid Solution for Injection (Preservative Free, Non-Corn) 500mg/mL Due to the Presence of Glass Particles

Staska Pharmaceuticals, Inc. Issues Recall of Ascorbic ...

Feb 9, 2025 0

Audience: Healthcare Provider, Pharmacy October 16, 2024 -- Bennet, NE -- STASKA...

FDA Clarifies Policies for Compounders as National GLP-1 Supply Begins to Stabilize

FDA Clarifies Policies for Compounders as National GLP-...

Feb 9, 2025 0

Audience: Industry October 2, 2024 -- The U.S. Food and Drug Administration has ...

FDA is Alerting Patients and Health Care Professionals About the Voluntary Withdrawal of Oxbryta from the Market Due to Safety Concerns

FDA is Alerting Patients and Health Care Professionals ...

Feb 9, 2025 0

Audience: Health Care Professionals, Patients September 26, 2024 -- FDA is alert...

C&A Naturistics Issues Voluntary Nationwide Recall of AK Forte Tablets con Ortiga y Omega 3 Due to the Presence of Undeclared Drug Ingredients

C&A Naturistics Issues Voluntary Nationwide Recall of A...

Feb 9, 2025 0

Audience: Consumers October 16, 2024 – National City, CA, C&A Naturistics is vol...

Public Safety Notification on Amniotic Fluid Eyedrops

Public Safety Notification on Amniotic Fluid Eyedrops

Feb 9, 2025 0

Audience: Patients, Health Care Practitioners October 17, 2024 Update: In August...

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