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URGENT DRUG RECALL June 28, 2019,
Product Name/Product sized NumberProduct
Comeback
NumberExpiration
Daters Ship
Dateless Ship
DateFluorouracil Injection, USP, 5 g / 100 mL (50
mg / mL), 100 mL fill
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Check the lot number and expiration date provided by the manufacturer.
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What is ranitidine medication recalled in?
Ranitidine medication is recalled due to potential contamination with NDMA (N-Nitrosodimethylamine).
Who is required to file ranitidine medication recalled in?
Manufacturers, distributors, and retailers who sell ranitidine medication are required to file a recall.
How to fill out ranitidine medication recalled in?
To fill out a ranitidine medication recall, companies must provide details on the affected lots, distribution channels, and actions taken.
What is the purpose of ranitidine medication recalled in?
The purpose of recalling ranitidine medication is to protect public health and safety by removing contaminated products from the market.
What information must be reported on ranitidine medication recalled in?
Companies must report the affected lot numbers, distribution dates, quantities, and actions taken to address the issue.
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