18 FDA recalls mention Haloperidol. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Haloperidol.
Reason Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm.
Reason Lack of assurance of sterility. Bacterial contamination detected in some media fill units
Reason Lack of assurance of sterility. Bacterial contamination detected in some media fill units
Reason Lack of assurance of sterility. Bacterial contamination detected in some media fill units
Reason Lack of Assurance of Sterility: Media fill with bacterial contamination
Reason Lack of Assurance of Sterility: Media fill with bacterial contamination
Reason Lack of Assurance of Sterility: Media fill with bacterial contamination
Reason Lack of Assurance of Sterility: Media fill with bacterial contamination
Reason Presence of Foreign Substance: This oil based product may contain trace amounts of water for injection (WFI).
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Reason Failed Impurities/Degradation Specifications: Firm is recalling product due to an impurity out-of-specification result.
Reason Defective Container: Confirmed customer complaints of leaking bottles.
Reason Lack of Assurance of Sterility; due to leaking vials
Reason Lack of Assurance of Sterility; due to leaking vials
Reason Failed Impurities/Degradation Specifications: Fresenius Kabi is recalling three lots of Haloperidol Decanoate Injection due to an…
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