US Drug Recall Register

Is Chloride recalled?

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.

Class II · Moderate risk Terminated

Premier Value

Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.

Product Quest Manufacturing LLC D-0046-2019
Class II · Moderate risk Terminated

Meijer

Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.

Product Quest Manufacturing LLC D-0042-2019
Class II · Moderate risk Terminated

Harmon Face Values

Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.

Product Quest Manufacturing LLC D-0040-2019
Class II · Moderate risk Terminated

FAMILY wellness

Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.

Product Quest Manufacturing LLC D-0038-2019
Class II · Moderate risk Terminated

DG health

Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.

Product Quest Manufacturing LLC D-0037-2019
Class II · Moderate risk Terminated

Discount Drug Mart

Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.

Product Quest Manufacturing LLC D-0036-2019
Class II · Moderate risk Terminated

CVS Health

Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.

Product Quest Manufacturing LLC D-0032-2019
Class II · Moderate risk Terminated

CVS Health

Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.

Product Quest Manufacturing LLC D-0031-2019
Class II · Moderate risk Terminated

CVS Health

Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.

Product Quest Manufacturing LLC D-0030-2019
Class II · Moderate risk Terminated

Rhinall

Reason CGMP Deviations: products manufactured under conditions that could impact its product quality.

Product Quest Manufacturing LLC D-0028-2019
Class II · Moderate risk Terminated

Dymista

Reason Presence of foreign substance: Potential for glass in the neck area of the glass bottles.

Mylan Pharmaceuticals Inc. NDC 0037-0245-23 D-1075-2018
Class II · Moderate risk Terminated

5 mg/mL Ephedrine Sulfate

Reason CGMP deviations: Product was released while a hood certification discrepancy was being investigated.

PharMEDium Services, LLC D-1044-2018
Class II · Moderate risk Terminated

10 mcg/mL Fentanyl Citrate

Reason CGMP deviations: Product was released while a hood certification discrepancy was being investigated.

PharMEDium Services, LLC D-1043-2018
Class III · Low risk Terminated

Fluconazole Injection

Reason Superpotent Drug: lots out of specification for elevated sodium chloride and fluconazole assay.

Renaissance Lakewood, LLC D-1033-2018
Class III · Low risk Terminated

Fluconazole Injection

Reason Failed Stability Specifications: lot out of specification for elevated water vapor.

Renaissance Lakewood, LLC NDC 36000-002-10 D-1032-2018
Class III · Low risk Terminated

Fluconazole Injection

Reason Superpotent Drug and Failed Stability Specifications: lot out of specification for elevated sodium chloride and elevated water vapor.

Renaissance Lakewood, LLC NDC 36000-003-06 D-1031-2018
Class II · Moderate risk Terminated

Metformin Hydrochloride Extended Release Tablets

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.

Sun Pharmaceutical Industries, Inc. NDC 62756-142-02 D-0924-2018
Class II · Moderate risk Terminated

Phenylephrine HCL 80mg in 0.9% Sodium Chloride 250 mL 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.

SCA Pharmaceuticals, LLC D-0905-2018
Class II · Moderate risk Terminated

Phenylephrine HCL 50 mg in 0.9% Sodium Chloride 250 mL 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.

SCA Pharmaceuticals, LLC D-0904-2018
Class II · Moderate risk Terminated

Phenylephrine HCL 20 mg in 0.9% Sodium Chloride 250 mL 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.

SCA Pharmaceuticals, LLC D-0903-2018
Class II · Moderate risk Terminated

Phenylephrine HCL 40 mg in 0.9% Sodium Chloride 250 mL 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.

SCA Pharmaceuticals, LLC D-0902-2018
Class II · Moderate risk Terminated

Phenylephrine HCL 10 mg in 0.9% Sodium Chloride 250 mL 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.

SCA Pharmaceuticals, LLC D-0901-2018
Class II · Moderate risk Terminated

Norepinephrine Bitartrate 16 mg

Reason Lack of Assurance of Sterility: SCA is conducting a voluntary recall of certain lots of sterile admixtures due to a potential for leakage.

SCA Pharmaceuticals, LLC D-0900-2018