Is Papaverine recalled?
322 FDA recalls mention Papaverine. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Papaverine.
Class II · Moderate risk Terminated Feb 21, 2019
Reason Lack of Processing Controls: Insanitary conditions observed during compounding of sterile drugs during recent FDA Inspection.
Class II · Moderate risk Terminated Feb 21, 2019
Reason Lack of Processing Controls: Insanitary conditions observed during compounding of sterile drugs during recent FDA Inspection.
Class II · Moderate risk Terminated Feb 21, 2019
Reason Lack of Processing Controls: Insanitary conditions observed during compounding of sterile drugs during recent FDA Inspection.
Class II · Moderate risk Terminated Sep 10, 2018
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated Sep 10, 2018
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated Sep 10, 2018
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated Sep 10, 2018
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated Sep 10, 2018
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated Sep 10, 2018
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated Sep 10, 2018
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated Sep 10, 2018
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated Sep 10, 2018
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated Sep 10, 2018
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated Sep 10, 2018
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated Jul 25, 2018
Reason Lack of Assurance of Sterility: Practices at firm may call into question the sterility of products intended to be sterile.
Class II · Moderate risk Terminated Jul 25, 2018
Reason Lack of Assurance of Sterility: Practices at firm may call into question the sterility of products intended to be sterile.
Class II · Moderate risk Terminated Jul 25, 2018
Reason Lack of Assurance of Sterility: Practices at firm may call into question the sterility of products intended to be sterile.
Class II · Moderate risk Terminated Jul 25, 2018
Reason Lack of Assurance of Sterility: Practices at firm may call into question the sterility of products intended to be sterile.
Class II · Moderate risk Terminated Jul 25, 2018
Reason Lack of Assurance of Sterility: Practices at firm may call into question the sterility of products intended to be sterile.
Class II · Moderate risk Terminated Jul 25, 2018
Reason Lack of Assurance of Sterility: Practices at firm may call into question the sterility of products intended to be sterile.
Class II · Moderate risk Terminated Jul 25, 2018
Reason Lack of Assurance of Sterility: Practices at firm may call into question the sterility of products intended to be sterile.
Class II · Moderate risk Terminated Apr 24, 2018
Reason Lack of assurance of sterility: Upon review of recent 3rd party environmental certification documentation, it was determined that airflow patterns…
Class II · Moderate risk Terminated Apr 24, 2018
Reason Lack of assurance of sterility: Upon review of recent 3rd party environmental certification documentation, it was determined that airflow patterns…
Class II · Moderate risk Terminated Apr 24, 2018
Reason Lack of assurance of sterility: Upon review of recent 3rd party environmental certification documentation, it was determined that airflow patterns…
Class II · Moderate risk Terminated Nov 16, 2017
Reason Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.