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West-ward Pharmaceutical Corp. recalls PredniSONE Tablets, USP, 20 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1477-01), b) 500-count tablets per

Recalled January 30, 2013 · FDA recall D-133-2013 · West-ward Pharmaceutical

Hazard
Presence of Foreign Substance: A complaint was received for black specks identified as stainless steel inclusions and cellulose with trace amounts of aluminum and iron-rich inclusions. · FDA Class II
Units
60,289 bottles
Sold at
Nationwide and Puerto Rico

Description

Presence of Foreign Substance: A complaint was received for black specks identified as stainless steel inclusions and cellulose with trace amounts of aluminum and iron-rich inclusions.

Product
PredniSONE Tablets, USP, 20 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1477-01), b) 500-count tablets per bottle (NDC 0143-1477-05), and c) 1000-count tablets per bottle (NDC 0143-1477-10), Rx only, Manufactured by: West-ward Pharmaceutical Corp., Eatowntown, NJ 07724.
Manufacturer(s)
West-ward Pharmaceutical Corp.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

West-ward Pharmaceutical Corp. recalls PredniSONE Tablets, USP, 20 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1477-01), b) 500-count tablets per | RecallWatchUSA