356 FDA recalls mention Fentanyl. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Fentanyl.
Reason Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Reason Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Reason Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Reason Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Reason Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
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 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 Assurance of Sterility
Reason Lack of Assurance of Sterility; The firm is recalling all sterile preparations that are within expiry due to deficient practices which may have an…
Reason Subpotent Drug
Reason Subpotent Drug
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