306 FDA recalls mention Bupivacaine. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Bupivacaine.
Reason Lack of Processing Controls; Environmental sampling revealed 1 CFU (Colony Forming Unit) identified as Talaromyces rotundus, a fungi.
Reason Lack of Processing Controls; Environmental sampling revealed 1 CFU (Colony Forming Unit) identified as Talaromyces rotundus, a fungi.
Reason Lack of Processing Controls; Environmental sampling revealed 1 CFU (Colony Forming Unit) identified as Talaromyces rotundus, a fungi.
Reason Lack of Processing Controls; Environmental sampling revealed 1 CFU (Colony Forming Unit) identified as Talaromyces rotundus, a fungi.
Reason Lack of Assurance of Sterility
Reason Lack of sterility assurance.
Reason Lack of Assurance of Sterility: SCA is conducting a voluntary recall of certain lots of sterile admixtures due to a potential for leakage.
Reason Lack of Assurance of Sterility: Potential leakage of bags.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack Of Assurance Of Sterility.
Reason Lack Of Assurance Of Sterility.
Reason Lack of Assurance of Sterility; product has the potential to leak.
Reason Lack of Assurance of Sterility; product has the potential to leak.
Reason Lack of Assurance of Sterility; product has the potential to leak.
Reason Lack of Assurance of Sterility; product has the potential to leak.
Reason Lack of Assurance of Sterility; product has the potential to leak.
Reason Lack of Assurance of Sterility; product has the potential to leak.
Reason Lack of Assurance of Sterility; product has the potential to leak.
Reason Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Reason Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Reason Labeling: Incorrect or Missing Lot and/or Exp Date
Reason Labeling: Incorrect or Missing Lot and/or Exp Date
Reason Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Reason Lack of Assurance of Sterility and Subpotent Drug: defect in glass vial prevented stopper from forming a seal allowing water to ingress and dilute…
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