85 FDA recalls mention Chlorhexidine. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Chlorhexidine.
Reason Lack of Assurance of Sterility: Product is being recalled because at labeled storage conditions of 30*C/75% Relative Humidity, there is the…
Reason Lack of Assurance of Sterility: Product is being recalled because at labeled storage conditions of 30*C/75% Relative Humidity, there is the…
Reason Microbial Contamination of Non-Sterile Product:.Product is being recalled because at labeled storage conditions of 30*C/75% Relative Humidity, growth…
Reason Microbial Contamination of Non-Sterile Product.Product is being recalled because at labeled storage conditions of 30*C/75% Relative Humidity, growth…
Reason Non-sterility.Product is being recalled because at labeled storage conditions of 30*C/75% Relative Humidity, growth of Aspergillus penicillioides, a…
Reason Non-sterility.Product is being recalled because at labeled storage conditions of 30*C/75% Relative Humidity, growth of Aspergillus penicillioides, a…
Reason cGMP deviations: The firm was notified of the manufacturer's expanded recall.
Reason cGMP Deviations; FDA inspection of manufacturing facility observed potential Burkholderia cepacia complex (BCC) contamination, inadequate cleaning…
Reason Microbial contamination of non-sterile products: Repackaged product was recalled by manufacturer because it was contaminated with the bacteria…
Reason Microbial Contamination of Non-sterile Products: contamination with Burkholderia lata.
Reason Discoloration.
Reason Non-sterility: Product is being recalled to climatic Zone IV regions of the world where at the labeled storage conditions of 30*C/75% Relative…
Reason Microbial Contamination of Non-Sterile Product: Product is being recalled to climatic Zone IV regions of the world where at the labeled storage…
Reason Microbial Contamination of Non-Sterile Products:Product is being recalled to climatic Zone IV regions of the world where at the labeled storage…
Reason Non-sterility: Product is being recalled to climatic Zone IV regions of the world where at the labeled storage conditions of 30*C/75% Relative…
Reason Microbial contamination of Non-Sterile Product; detection of the gram-negative bacillus Serratia marcescens in certain API batches
Reason Non-Sterility: Product is being recalled due to presence of Aspergillus Penicilloides
Reason Non-Sterility: Product is being recalled due to presence of Aspergillus Penicilloides
Reason Non-Sterility: Product is being recalled due to presence of Aspergillus Penicilloides
Reason CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.
Reason Labeling: Not Elsewhere Classified: due to a labeled declaration of; Store at 15¿C to 30¿C (59¿F to 86¿F) which differs from the original…
Reason Subpotent Drug: Product crystallization with accompanying low out of specification results for chlorhexidine assay.
Reason Subpotent Drug: Product crystallization with accompanying low out of specification results for chlorhexidine assay.
Reason Subpotent Drug: Product crystallization with accompanying low out of specification results for chlorhexidine assay.
Reason Labeling; Label Mixup; the immediate package is labeled incorrectly as Chloroprep Onestep (Clear), however, the correct label should be Chloroprep…
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