6 FDA recalls mention Drospirenone. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Drospirenone.
Reason Failed Stability Specification and Failed Impurities/Degradation Specifications: out of specification for inactive content ascorbic acid and…
Reason Subpotent Drug
Reason Failed dissolution specifications : failed results at the 3-month stability time point.
Reason Contraceptive Tablets Out of Sequence: Missing or incorrect tablet placement.
Reason Failed Tablet/Capsule Specification; tablet breakage while pushing through the blister pack (dispenser) .
Reason Tablet/Capsule Imprinted with Wrong ID; a portion of the tablets could contain the incorrect debossing on one side of the tablet U2 instead of U3.
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