Yes — there is an active recall. 69 ongoing FDA recalls mention Testosterone (411 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Testosterone. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Reason CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure…
Reason CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure…
Reason CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure…
Reason CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure…
Reason Subpotent Drug: Out of specification assay result in Esterified Estrogen and Methyltestosterone tablets.
Reason Subpotent Drug: Out of specification assay result in Esterified Estrogen and Methyltestosterone tablets.
Reason Temperature Abuse: Prolonged exposure to temperatures outside of labeled storage conditions.
Reason Temperature Abuse: Prolonged exposure to temperatures outside of labeled storage conditions.
Reason CGMP Deviations
Reason Marketed without an Approved NDA/ANDA; FDA analysis found the presence of undeclared tadalafil, sildenafil and/or their analogues and Flibanserin
Reason CGMP deviations: Lots were recalled due to sub-potency and cGMP violations.
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