195 FDA recalls mention Epinephrine. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Epinephrine.
Reason Incorrect excipient: Product was compounded in 250 mL 5% Dextrose instead of 250 mL 0.9% Sodium Chloride
Reason Labeling Incorrect Instructions: This recall has been initiated because the Instructions for Use included in the Epi-Safe Kits for the Epi-Safe…
Reason Labeling Incorrect Instructions: This recall has been initiated because the Instructions for Use included in the Epi-Safe Kits for the Epi-Safe…
Reason Labeling: Incorrect or missing Lot and/or Exp Date:The Kit is incorrectly labeled as expiring May 2018 however the correct expiration date is May…
Reason Subpotent drug: During testing of the retention sample, the firm discovered that the product was sub-potent.
Reason Subpotent Drug: Product may not have the active ingredient present in the bag.
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: SCA is conducting a voluntary recall of certain lots of sterile admixtures due to a potential for leakage.
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 Assurance of Sterility: Potential leakage of bags.
Reason Lack of Assurance of Sterility: Potential leakage of bags.
Reason Lack of Assurance of Sterility: Potential leakage of bags.
Reason Lack of Assurance of Sterility: Potential leakage of bags.
Reason Lack of Assurance of Sterility: Potential leakage of bags.
Reason Lack of Assurance of Sterility: Potential leakage of bags.
Reason Lack of Assurance of Sterility.
Reason Lack of Assurance of Sterility.
Reason Lack of sterility assurance: resulting from use of a damaged sterilizing filter for nitrogen used in the manufacturing process.
Reason Lack of sterility assurance: Microbial growth detected during a routine simulation of the manufacturing process. No batches of distributed product…
Reason Lack of Sterility Assurance.
Reason Lack of Sterility Assurance.
Reason Lack of Sterility Assurance.
Reason Lack of Assurance of Sterility; product has the potential to leak.
Reason Lack of Assurance of Sterility; product has the potential to leak.
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