FDA MedWatch Class 2 Device Recall: AMIA Automated PD Cycler

Date Initiated by Firm

July 12, 2018

Create Date

August 02, 2018

FDA MedWatch: AuroMedics Pharma LLC Issues Voluntary Nationwide Recall of Piperacillin and Tazobactam

August 1, 2018

Hospira Issues Voluntary Nationwide Recall of Daptomycin for Injection Lyophilized Powder for Solution, Due to Infusion Reactions

Hospira Issues Voluntary Nationwide Recall of Daptomycin for Injection Lyophilized Powder for Solution, Due to Infusion Reactions

Fluoroquinolone Antibiotics: FDA Requires Labeling Changes

ISSUE: FDA is strengthening the current warnings in the prescribing information that fluoroquinolone antibiotics may cause significant decreases in blood sugar and certain mental health side effects. 

CDC Health Advisory: Outbreak of Hepatitis A Virus (HAV) Infections among Persons Who Use Drugs and Persons Experiencing Homelessness

June 11, 208

Original content : https://emergency.cdc.gov/han/han00412.asp

Apotex Corp. Issues Voluntary Nationwide Recall of Piperacillin and Tazobactam For Injection

May 14, 2018

Ampicillin and Sulbactam for Injection USP, 3 g Single-Dose Vials by AuroMedics Pharma: Recall - Presence of Red Particulate Matter

May 8, 2018

Piperacillin and Tazobactam for Injection, USP 3.375 g Vials by AuroMedics Pharma: Recall - Vials Contain Particulate Matter

May 8, 2018

Class 2 Device Recall 2008 Series Hemodialysis Machine

Date Initiated by Firm: December 14, 2017

Create Date: March 20, 2018

Recall Status1:Open3, Classified

Recall Number: Z-1278-2018

Recall Event ID: 79478

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