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 Failed Impurities/Degradation Specifications: High out of specification impurity test results were obtained during stability testing.
Reason Failed Impurities/Degradation Specifications: High out of specification impurity test results were obtained during stability testing.
Reason Failed Impurity/Degradation Specification; out-of-specification result for one individual unknown impurity at the 24-month room temperature stability…
Reason Presence of Particulate; red and black particulate within the solution and embedded within the plastic vial identified as iron oxide
Reason Superpotent Drug: Product contains twice the stated amount of midazolam.
Reason CGMP Deviations; laboratory testing was not followed in accordance with GMP requirements
Reason Failed Dissolution Specifications: Stability results found the product did not meet the drug release dissolution specifications.
Reason Failed Dissolution Specifications: Stability results found the product did not meet the drug release dissolution specifications.
Reason Defective container: Product distributed without inner seal on bottles.
Reason Defective container: Product distributed without inner seal on bottles.
Reason Presence of Particulate Matter Perrigo is recalling seven lots of Clindamycin Palmitate Hydrochloride for Oral Solution 75mg/5ml.
Reason Failed Dissolution Specification: Out of Specification dissolution results at 12 month interval.
Reason Lack of Assurance of Sterility:Solution leaking through the port cover of the primary container, which was identified during a retain sample visual…
Reason Subpotent Drug: Drug potency was compromised during shipment.
Reason CGMP Deviations: Ethambutol Hydrochloride Tablets, USP, 400 mg were manufactured using unapproved material: the incorrect gelatin excipient than…
Reason Lack of Assurance of Sterility; potential leakage from administrative port.
Reason Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria was found, Serratia liquefaciens.
Reason Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria was found, Serratia liquefaciens.
Reason Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria was found, Serratia liquefaciens.
Reason Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria was found, Serratia liquefaciens.
Reason Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria was found, Serratia liquefaciens.
Reason Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria was found, Serratia liquefaciens.
Reason Failed impurities/degradation specifications; out of specification for the known impurity 4-chlorobenzophenone.
Reason Lack of Assurance of Sterility: The firm expanded the recall to other injectable products due to lack of assurance of sterility from poor aseptic…
Reason Labeling: Wrong Bar Code; Bar code scans as 0.15% Potassium Chloride in 0.9% Sodium Chloride (20 mEq K/liter).
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