TEST CYPIONATE 200MG/ANASTROZOLE 1.5MG/DUTASTERIDE 1.5MG/ML IN OIL INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950…
Reason Lack of assurance of sterility
54 FDA recalls mention Anastrozole. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Anastrozole.
Reason Lack of assurance of sterility
Reason Lack of assurance of sterility
Reason Lack of assurance of sterility
Reason Lack of assurance of sterility
Reason Lack of assurance of sterility
Reason Lack of assurance of sterility
Reason Lack of assurance of sterility
Reason Lack of assurance of sterility
Reason Lack of Processing Controls (lack of assurance of conformity to specifications).
Reason GMP Deviations: Potential cross contamination due to cleaning procedure failure.
Reason GMP Deviations: Potential cross contamination due to cleaning procedure failure.
Reason CGMP Deviations: Cross Contamination with other products due to CGMP cleaning failure.
Reason CGMP Deviations: Cross Contamination with other products due to CGMP cleaning failure.
Reason Lack of Assurance of Sterility
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure…
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.
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.
Reason Lack of Assurance of Sterility
Reason Superpotent and Subpotent drugs
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