Azithromycin for Injection USP Vial, 500 mg per vial, Rx only, Manufacturer: Auromedics Pharma LLC, NDC 55150-174-10
Check against the official notice below — it lists the full affected range.
McKesson Medical-Surgical Inc. is recalling Azithromycin for Injection USP 500 mg vials manufactured by Auromedics Pharma LLC due to temperature abuse violations of good manufacturing practices (cGMP). The recall affects 13 cartons containing 10 vials each that were distributed nationwide across the United States. Because McKesson cannot identify which specific lot numbers were received by individual customers, affected parties should refer to the distribution dates included in their recall notification letters to determine if their product may be impacted.
The source does not specify a remedy or recommended action for consumers who may have received affected 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: 13 carton/10 vials each 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.