NORepinephrine 4 mg in 0.9% Sodium Chloride 250 mL from Stock, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205…
Reason Lack of Assurance of Sterility; product has the potential to leak.
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 Lack of Assurance of Sterility; product has the potential to leak.
Reason Lack of Assurance of Sterility; product has the potential to leak.
Reason GMP Deviation; A foreign stopper was observed during packaging of a lot of product.
Reason Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication
Reason Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication
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 Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Subpotent Drug; confirmed results by FDA analysis after customer complaints of discoloration
Reason Subpotent Drug; confirmed results by FDA analysis after customer complaints of discoloration
Reason Defective Delivery System; potential to have inaccurate dosage delivery
Reason Defective Delivery System; potential to have inaccurate dosage delivery
Reason Discoloration
Reason Discoloration
Reason Subpotent drug.
Reason Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
Reason Presence of Particulate Matter: The firm produced products using 0.9% Sodium Chloride Injection, USP or 5% Dextrose Injection, USP which were…
Reason Presence of Particulate Matter: The firm produced products using 0.9% Sodium Chloride Injection, USP or 5% Dextrose Injection, USP which were…
Reason Presence of Particulate Matter: The firm produced products using 0.9% Sodium Chloride Injection, USP or 5% Dextrose Injection, USP which were…
Reason Penicillin Cross Contamination: All lots of all products repackaged and distributed between 01/05/12 and 02/12/15 are being recalled because they…
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