5 FDA recalls mention Ramipril. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Ramipril.
Reason CGMP Deviations: Active pharmaceutical ingredient was sourced from an unapproved vendor
Reason CGMP Deviations: Active pharmaceutical ingredient was sourced from an unapproved vendor
Reason CGMP Deviations: Active pharmaceutical ingredient was sourced from an unapproved vendor
Reason Labeling: Incorrect or Missing Lot And/or Exp Date: Bottles labeled with the incorrect expiration date of 03/18 rather than 09/17.
Reason Labeling:Label Mixup; RAMIPRIL, Capsule, 2.5 mg, Rx only may be potentially mislabeled as PROPAFENONE HCL, Tablet, 150 mg, NDC 00591058201…
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