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Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.
Yes — there is an active recall. 326 ongoing FDA recalls mention Chloride (1,994 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Chloride. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed.
Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.
Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.
Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.
Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.
Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.
Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.
Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.
Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.
Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.
Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.
Reason Presence of foreign substance: Potential for glass in the neck area of the glass bottles.
Reason CGMP deviations: Product was released while a hood certification discrepancy was being investigated.
Reason CGMP deviations: Product was released while a hood certification discrepancy was being investigated.
Reason Superpotent Drug: lots out of specification for elevated sodium chloride and fluconazole assay.
Reason Failed Stability Specifications: lot out of specification for elevated water vapor.
Reason Superpotent Drug and Failed Stability Specifications: lot out of specification for elevated sodium chloride and elevated water vapor.
Reason Presence of foreign substance: One lot fo Metformin Hydrochloride Extended Release Tablets, USP, 500 mg (500 Count) contains foreign matter identified as a piece of rubber glove detected in one tablet.
Reason CGMP Deviations: Syringes were filled with 19mL of potassium chloride when the labels displayed a fill of 20mL.
Reason Subpotent Drug: final drug concentration is subpotent as compared to the concentration indicated on the label.
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: 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.
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