Geodon for injection (ziprasidone mesylate), 20 mg/mL, 1 mL single dose vial, Rx only, MFG: Viatris, NDC 0049-3920-83
Check against the official notice below — it lists the full affected range.
McKesson Medical-Surgical Inc. is recalling Geodon for injection (ziprasidone mesylate), 20 mg/mL, 1 mL single dose vials manufactured by Viatris. The recall affects one carton containing 10 vials that were distributed nationwide in the United States. The product is being recalled due to Good Manufacturing Practice (cGMP) deviations involving temperature abuse during storage or handling.
McKesson Medical-Surgical is unable to identify the specific lot number for the recalled product received by individual customers. Instead, McKesson has sent letters to affected customers that include the distribution date and the timeframe when the impacted product may have been shipped to them. The recall source does not specify a remedy or corrective action for consumers who may have received this product.
Written by software from the official notice below. Not reviewed by a lawyer.
cGMP deviations: Temperature abuse
Reason for recall: cGMP deviations: Temperature abuse Distribution: USA nationwide. Quantity: 1 carton/10 vials Lot/code info: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
Official record: FDA (Drug enforcement) ↗
Republished from the official source above; details can change — the source record controls.