4 FDA recalls mention Lubiprostone. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Lubiprostone.
Reason Labeling: Label mix-up. Amitiza 8 mcg capsules are being recalled because 24 mcg capsules were found in a 8 mcg trade 60 ct. bottle. Amitiza 24 mcg…
Reason Labeling: Label mix-up. Amitiza 8 mcg capsules are being recalled because 24 mcg capsules were found in a 8 mcg trade 60 ct. bottle. Amitiza 24 mcg…
Reason Failed Impurities/Degradation Specifications:Elevated levels of a known impurity in the 20-month stability sample testing.
Reason Labeling: Label Mixup; LUBIPROSTONE Capsule, 24 mcg may be potentially mislabeled as ARIPiprazole, Tablet, 2 mg, NDC 59148000613, Pedigree…
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.