Yes — there is an active recall. 61 ongoing FDA recalls mention East (1,061 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of East. “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 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 Failed Tablet/Capsules Specifications: pharmacists complaints for bottles containing melted capsules.
Reason Failed Stability Specifications: Out of Specification results obtained for preservative Methylparaben content.
Reason Presence of Foreign Tablet/Capsule; Amoxicillin 500 mg was found in bottles of Penicillin V potassium 500 mg
Reason Failed Tablet/Capsule Specifications: Capsule shell (s) opening inside the bottle The Initial reports stated one or two capsules in a bottle count…
Reason Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
Reason Lack of Assurance of Sterility
Reason CGMP Deviations: Failure of the manufacturer, Wockhardt Ltd, to adequately investigate customer complaints.
Reason Non-Sterility: Out of specification results for the sterility test for microbial contamination.
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