STAQ Pharma recalled Ketamine Hydrochloride injections distributed nationwide in the United States. The labeling has incorrect or missing lot and expiration date information. Stop using the product and contact STAQ Pharma or your healthcare provider for guidance.
Labeling: Incorrect or Missing Lot and/or Exp Date
Consumers and healthcare providers should stop using this product immediately. Contact STAQ Pharma, Inc. or your healthcare provider for guidance. Notification method: Letter
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Ketamine Hydrochloride injection is used in clinical settings as an anesthetic or analgesic adjunct. The product is supplied in a 50 mL syringe with labeled strength of 50 mg per 5 mL.
The defect is labeling. Incorrect or missing lot and expiration date information can hinder traceability and dosing accuracy, potentially affecting patient safety.
This recall is not described as part of a broader industry pattern in the notice.
Healthcare providers must verify labeling before use. The recall can create administrative burden and potential delays in patient care while traces are completed.
FDA enforcement page link and STAQ Pharma recall communications. Manufacturer address: 14135 E 42nd Ave, Denver, CO.
No specific timeline provided for resolution or refunds. Follow STAQ Pharma guidance.
Keep a copy of the recall notice, record lot 25156673A and expiry 02FEB2026, and save all correspondence with the manufacturer.
Ketamine Hydrochloride, 50 mg/5 mL (10 mg/mL), in a 50 mL syringe. Brand STAQ Pharma Inc. NDC 73177-0156-02. Lot 25156673A. Expiry 02FEB2026. Distributed nationwide in the U.S.
No injuries or incidents have been reported.
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