Yes — there is an active recall. 19 ongoing FDA recalls mention Choline (151 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Choline. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed.
Reason Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for the lot number and/or expiration date to be faded or missing from the primary label…
Reason Superpotent Drug: The vitamin supplement contains an extremely high level of vitamin D3 (Cholecalciferol).
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility; The firm is recalling all sterile preparations that are within expiry due to deficient practices which may have an…
Reason Lack of Assurance of Sterility; The firm is recalling all sterile preparations that are within expiry due to deficient practices which may have an…
Reason Lack of Assurance of Sterility; The firm is recalling all sterile preparations that are within expiry due to deficient practices which may have an…
Reason Subpotent Drug: trace amounts of methylcobalamin in compounded drug.
Reason Stability data does not support expiry.
Reason Stability data does not support expiry.
Reason Stability data does not support expiry.
Reason Stability data does not support expiry.
Reason Stability data does not support expiry.
Reason Stability data does not support expiry.
Reason Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Reason Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Reason Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Reason Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Reason Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
Reason Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
Reason Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
Reason Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
Reason Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
Reason Good Manufacturing Practices Deviations: The product has an active pharmaceutical ingredient from an unapproved source.
Reason Lack of Assurance of Sterility: Lack of sterility assurance in compounded aseptically filled injectable products.
Reason Lack of Assurance of Sterility: Lack of sterility assurance in compounded aseptically filled injectable products.
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