Adamis Pharmaceuticals Corporation Issues Nationwide Voluntary Recall of SYMJEPI® (Epinephrine) Injection for Potential Manufacturing...

MedWatch - The FDA Safety Information and Adverse Event Reporting Program TOPIC: 0.9% Sodium Chloride for Injection USP, 250 mL in Excel...

FOR IMMEDIATE RELEASE – January 26, 2022 – East Windsor, New Jersey, AuroMedics Pharma LLC has initiated a voluntary recall of lot number...

TOPIC: Vaporizer Sevoflurane Maquet Filling for Flow Family Anesthesia Systems by Getinge: Class I Recall - Due to a Risk of Harmful...

SterRx, LLC today announced the voluntary nationwide recall of approximately 240 lots within their expiry period due to equipment and...

The FDA recommends that health care facilities and providers do not purchase or use imported medical gloves from companies included on...

Summary Company Announcement Date:September 25, 2021 FDA Publish Date:September 26, 2021 Product Type:Drugs Reason for Announcement:Loss...

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or...

Company Announcement Minneapolis, Minnesota, IntegraDose Compounding Services is voluntarily recalling nine lots, listed in the table...

Teligent Pharma, Inc.’s Issues Voluntary Recall of Lidocaine HCl Topical Solution 4% (Lot # 14218, Exp. 09/2022) Due to Super Potency...

MedWatch - The FDA Safety Information and Adverse Event Reporting Program TOPIC: Select Monoject Flush Prefilled Saline Syringes By...

MedWatch - The FDA Safety Information and Adverse Event Reporting Program TOPIC: Sodium Bicarbonate in 5% Dextrose Injection 150 mEq per...

TOPIC: Surgical Procedure Packs by DeRoyal Industries: Class I Recall - Due to Mislabeled Lidocaine AUDIENCE: Patient, Health...

BD Announces the Voluntary Recall of Specified Lots of ChloraPrep™ Hi-Lite Orange™ 26 mL Applicator in the United States and U.S....

Sagent Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Phenylephrine Hydrochloride Injection, USP, 10 mg/mL Due to Potential...

Meitheal Pharmaceuticals, Inc. (“Meitheal”), announced today that it is voluntarily recalling one (1) lot of Cisatracurium Besylate...

MedWatch - The FDA Safety Information and Adverse Event Reporting Program TOPIC: AUDIENCE: Patient, Health Professional, Risk Manager,...

https://www.fda.gov/drugs/drug-safety-and-availability/fda-alerts-perrigos-voluntary-albuterol-inhaler-recall?utm_medium=email&utm_source...

Fresenius Kabi USA is voluntarily recalling two lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg/50 mL (4 mcg /...

If your email program has trouble displaying this email, view it as a web page. Mylan Initiates Voluntary Nationwide Recall of One Lot of...