13 FDA recalls mention Diazepam. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Diazepam.
Reason Failed Impurities/Degradation Specifications: Out of specification results for related substances.
Reason Lack of Assurance of Sterility
Reason Labeling: Incorrect or Missing Lot and/or Exp Date: Product distributed without a lot number or expiration date on the outer carton.
Reason Crystallization: Product contains particulate identified to be crystallized active ingredient.
Reason Lack of Assurance of Sterility: Martin Avenue Pharmacy, Inc. is conducting a voluntary recall of all compounded sterile preparations within expiry…
Reason Lack of assurance of sterility: ineffective crimp on fliptop vials that may result in leaking at the neck of the vials.
Reason Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Reason Lack of Assurance of Sterility; FDA inspectional findings resulted in concerns associated with quality control procedures that impacted sterility…
Reason Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
Reason Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Reason Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Reason Impurities/Degradation Products: High Out of Specification levels for carbostyril, a known degradation product of diazepam.
Reason Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all Sterile Human Drugs distributed between 11/21/2011 and 05/21/2012 because…
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