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Home > Recalled Products > Drugs > Contamination > Par Pharmaceutical Mycophenolate Mofetil For Injection

Recall: Par Pharmaceutical Mycophenolate Mofetil For Injection


On 2019-05-01, the FDA announced that Par Pharmaceutical is conducting a recall on Mycophenolate Mofetil For Injection due to possible contamination with . The recalled products were sold under the brand name(s) Par Pharmaceutical during an unspecified time period throughout the regions shown in the map below.

In recent months, there have been 4 drugs recalls due to potential contamination, including losartan potassium tablets, usp; losartan potassium and hydrochlorothiazide tablets, usp, baby cough syrup + mucus and more. Additionally, there have been 26 drug and medical device recalls due to other health hazards as well as 77 food recalls.

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Mycophenolate Mofetil for Injection, USP, 500mg/vial
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Company Contact Information:

Name: Par Pharmaceutical

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Detailed Recall Information

Regions Where Sold: Nationwide

Product Description: Mycophenolate Mofetil for Injection

Brand Name(s): Par Pharmaceutical

Reason for Recall: Foreign Material Contamination

Official Recall Date: 2019-05-01


Additional information provided by the

Endo International plc, announced today that one of its operating companies, Par Pharmaceutical, Inc., is voluntarily recalling one lot of Mycophenolate Mofetil for Injection, USP to the hospital and retail pharmacy level. One vial of product was observed containing a glass fragment after reconstitution. Read More.

More information may be available at

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Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.

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