11 FDA recalls mention Prednisone. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Prednisone.
Reason Presence of foreign tablet: 2.5 mg tablet in a 20 mg bottle of Prednisone Tablets
Reason CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Reason Labeling: Label Mix Up: bottle labeled to contain Prednisone Tablets, USP 2.5 mg actually contained Prednisone Tablets, USP 10 mg
Reason Failed Tablet/Capsule Specifications: Discovery of an underweight tablet.
Reason Labeling: Not elsewhere classified. NDC number is incorrect on the container.
Reason Penicillin Cross Contamination: All lots of all products repackaged and distributed between 01/05/12 and 02/12/15 are being recalled because they…
Reason Labeling: Label Mixup:predniSONE, Tablet, 20 mg may have potentially been mislabeled as the following drug: methylPREDNISolone, Tablet, 4 mg, NDC…
Reason Labeling: Missing Label; missing label on blister card
Reason Presence of Foreign Substance(s); Perrigo has been notified of a recall by the manufacturer of this product, West-Ward Pharmaceuticals. This is a…
Reason Presence of Foreign Substance: Tablets are being recalled due to gray defects identified in the tablets.
Reason Presence of Foreign Substance: A complaint was received for black specks identified as stainless steel inclusions and cellulose with trace amounts of…
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