12 FDA recalls mention Misoprostol. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Misoprostol.
Reason Labeling: Label Mix-Up: bottle labeled as Diclofenac Sodium and Misoprostol 75 mg/0.2 mg contained Diclofenac Sodium and Misoprostol 50 mg/0.2 mg…
Reason Failed Impurities/Degradations Specifications; Out of specification results for two known degradation products and total impurities at 18 months
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 Failed Tablet/Capsule Specifications: Presence of split or broken tablets.
Reason Failed Tablet/Capsule Specifications: Recall due to complaints of split or broken tablets.
Reason Failed Tablet/Capsule Specifications: Recall due to complaints of split or broken tablets.
Reason Failed Tablet/Capsule Specifications: Split tablets were found in the 12-month stability samples.
Reason Labeling:Label Mixup; MISOPROSTOL Tablet, 200 mcg may be potentially mislabeled as PROPRANOLOL HCL, Tablet, 10 mg, NDC 23155011001, Pedigree…
Reason Labeling: Label Mixup; MISOPROSTOL Tablet, 100 mcg may be potentially mislabeled as QUINAPRIL HCL, Tablet, 10 mg, NDC 59762502001, Pedigree…
Reason Failed Tablet/Capsule Specifications: Broken tablets
Reason Failed Tablet/Capsule Specifications: Broken tablets
Reason Tablet Separation: The manufacturer of Arthrotec had recalled the lots that were used to re-package this product because they may contain broken…
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