FDA recall record

Fresenius Kabi USA Magnesium Sulfate Injection, USP, 50% (25 grams/50 mL), For IM or IV Use recall — FDA D-920-2013

Presence of Particulate Matter: Glass particulate matter was observed in a retention sample during an annual review.

Class Iclassification
D-920-2013official record ID
Sep 4, 2013report date

Recall record at a glance

Official recordD-920-2013
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmFresenius Kabi USA, LLC
Report dateSep 4, 2013
Recall initiation dateMay 25, 2013
Quantity15,625 vials
LocationLake Zurich, IL, United States

Official product description

Magnesium Sulfate Injection, USP, 50% (25 grams/50 mL), For IM or IV Use, 50 mL, Single Dose Vial, Rx only, Preservative Free, APP Pharmaceuticals, LLC, Schaumburg, IL, 60173, NDC 63323-064-50

Why the product was recalled

Presence of Particulate Matter: Glass particulate matter was observed in a retention sample during an annual review.

Distribution information

Nationwide

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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