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 Lack of Sterility Assurance: The product has the potential to leak at the administrative port.
Reason Labeling: Label mix-up; bottles were incorrectly labeled as 10 mL instead of correctly labeled as 4 mL
Reason Failed Impurities/Degradation Specifications: the manufacturer, recalled product due to slightly above specification results for a Related Compound…
Reason Failed Impurities/Degradation Specifications: A stability lot was out of specification for a known impurity at the 8 month Controlled Room…
Reason Failed Impurities/Degradation Specifications: Out of specification for unknown impurity.
Reason Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Reason Lack of Assurance of Sterility; increased complaints received for leaks
Reason Lack of Assurance of Sterility. Complaints were receive of missing closures and/or leaks which may compromise product sterility.
Reason Microbial Contamination of a Non-Sterile Product: Kit component is contaminated with Burkholderia multivorans.
Reason Presence of Particulate Matter: Confirmed finding of human hair floating in IV solution.
Reason Presence of Foriegn Substance: Plastic cap closure particulates may be present in the product.
Reason Subpotent Drug
Reason Subpotent Drug
Reason Correct Labeled Product Mispack: Ifosfamide Injection 50 mg/mL, 60 mL, correctly labeled vial may have been mis-packaged in a carton labeled…
Reason Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due…
Reason Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due…
Reason Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due…
Reason Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due…
Reason Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due…
Reason Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due…
Reason Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due…
Reason Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due…
Reason Subpotent Drug and Failed Impurities/Degradation Specifications
Reason Presence of Particulate Matter; Hospira has identified the particulate as a human hair, sealed in the bag at the additive port area.
Reason Subpotent Drug
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