LX Bioboost Plus
Lack of Assurance of Sterility
Yes — there is an active recall. 14 ongoing FDA recalls mention Methionine (71 total). Check the affected lots below.
Most common reason: Sterility / contamination (62 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Methionine. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of assurance of sterility.
Lack of assurance of sterility.
Lack of assurance of sterility.
Super Potent and Failed Reconstitution Time
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of processing controls
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Sterility Assurance.
Lack of assurance of sterility for injectables and solutions intended to be sterile.
Lack of sterility assurance.
Lack of sterility assurance.
Lack of assurance of sterility: Upon review of recent 3rd party environmental certification documentation, it was determined that airflow patterns may not be sufficient to support the aseptic production of certain injectable drug products.
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
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