4 FDA recalls mention Bismuth. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Bismuth.
Reason CGMP Deviations: product held outside appropriate storage temperature conditions.
Reason Labeling: Incorrect or Missing Lot and/or Exp Date - the label contains an incorrect Exp Date.
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: BISMUTH SUBSALICYLATE, CHEW Tablet, 262 mg may have potentially been mislabeled as the following drug: IRBESARTAN, Tablet…
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