Fresenius Kabi USA, LLC recalls Magnesium Sulfate Injection, USP, 50% (25 grams/50 mL), For IM or IV Use, 50 mL, Single Dose Vial, Rx only, Preservative
Recalled September 4, 2013 · FDA recall D-920-2013 · Fresenius Kabi USA
Hazard
Presence of Particulate Matter: Glass particulate matter was observed in a retention sample during an annual review. · FDA Class I
Units
15,625 vials
Sold at
Nationwide
Description
Presence of Particulate Matter: Glass particulate matter was observed in a retention sample during an annual review.
Product
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
Manufacturer(s)
Fresenius Kabi USA, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →