Class II · Moderate risk Terminated
Potassium PHOSphate in 0.9% Sodium Chloride Injection
Reason Lack of Assurance of Sterility; media fill failure at manufacturer
FDA Drug Recalls
11,815 recalls · Class II, newest first
Class II · Moderate risk Terminated
Potassium PHOSphate in 5% Dextrose Injection
Reason Lack of Assurance of Sterility; media fill failure at manufacturer
Class II · Moderate risk Terminated
Potassium PHOSphate in 0.9% Sodium Chloride Injection
Reason Lack of Assurance of Sterility; media fill failure at manufacturer
Class II · Moderate risk Terminated
Potassium PHOSphate in 0.9% Sodium Chloride Injection
Reason Lack of Assurance of Sterility; media fill failure at manufacturer
Class II · Moderate risk Terminated
Potassium PHOSphate in 0.9% Sodium Chloride Injection
Reason Lack of Assurance of Sterility; media fill failure at manufacturer
Class II · Moderate risk Terminated
Potassium PHOSphate in 5% Dextrose Injection
Reason Lack of Assurance of Sterility; media fill failure at manufacturer
Class II · Moderate risk Terminated
Potassium PHOSphate in 0.9% Sodium Chloride Injection 20 mMol in…
Reason Lack of Assurance of Sterility; media fill failure at manufacturer
Class II · Moderate risk Terminated
Potassium PHOSphate in 0.9% Sodium Chloride Injection 15 mMol in…
Reason Lack of Assurance of Sterility; media fill failure at manufacturer
Class II · Moderate risk Terminated
Potassium PHOSphate in 0.9% Sodium Chloride Injection
Reason Lack of Assurance of Sterility; media fill failure at manufacturer
Class II · Moderate risk Terminated
Succinylcholine Chloride Injection
Reason Lack of Assurance of Sterility; media fill failure at manufacturer
Class II · Moderate risk Terminated
Timolol-Brimonidine-Dorzolamide-Latanoprost
Reason Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier
Class II · Moderate risk Terminated
Timolol-Latanoprost PF Solution
Reason Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier
Class II · Moderate risk Terminated
Latanoprost PF Solution
Reason Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier
Class II · Moderate risk Terminated
Curcumin Emulsion 10mg/ml Injection
Reason Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier
Class II · Moderate risk Terminated
Potassium Phosphate
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Potassium Phosphate
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Potassium Phosphate
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Quelicin
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Potassium PHOSphate added to 0.9% Sodium Chloride 250 mL Bag 30 mMol
Reason Lack of sterility assurance
Class II · Moderate risk Terminated
Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 15 mMol
Reason Lack of sterility assurance
Class II · Moderate risk Terminated
Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 15 mMol
Reason Lack of sterility assurance
Class II · Moderate risk Terminated
Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 10 mMol
Reason Lack of sterility assurance
Class II · Moderate risk Terminated
Cyclobenzaprine HCl Tablets
Reason Labeling; Label Mix up; cartons labeled as Amantadine HCl 100 mg Capsules contain unit dose blister cards of Cyclobenzaprine HCl Tablet, USP 5 mg
Class II · Moderate risk Terminated
Amantadine HCl Capsules
Reason Labeling; Label Mix up; cartons labeled as Amantadine HCl 100 mg Capsules contain unit dose blister cards of Cyclobenzaprine HCl Tablet, USP 5 mg
Class II · Moderate risk Terminated
Succinylcholine Chloride
Reason Lack Of Assurance Of Sterility: voluntary recall initiated by the commercial supplier