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Hospira Issues A Voluntary Nationwide Recall of One Lot of Metoclopramide Injection, USP, and two lots of ondansetron injection, USP, due to Glass (Glass Strands) particulate caused by glass supplier defect
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Document Date: 2014-11-25 12:02:47


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City

LAKE FOREST / /

Company

IMMEDIATE RELEASE HOSPIRA ISSUES A VOLUNTARY NATIONWIDE / Hospira Inc. / HOSPIRA ISSUES A VOLUNTARY NATIONWIDE / Stericycle / /

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Event

Product Issues / Product Recall / /

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IndustryTerm

manufacturing glass defect / Replacement product / healthcare costs / infusion technologies / /

MedicalCondition

thrombophlebitis / shortness of breath / local inflammation / nausea / fever / pain / vomiting / cardiac and renal disease / macrovascular disease / tachycardia / /

MedicalTreatment

surgery / /

Organization

U.S. Food and Drug Administration / /

Person

LOT OF METOCLOPRAMIDE / /

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Product

This / VOLUNTARY NATIONWIDE / METOCLOPRAMIDE / ONDANSETRON / lot of Metoclopramide Injection / /

ProvinceOrState

Illinois / /

Technology

infusion technologies / /

URL

www.fda.gov/medwatch/report.htm / www.hospira.com / www.fda.gov/MedWatch/getforms.htm / /

SocialTag