Depo-Medrol (methylprednisolone acetate injectable suspension, USP) 80mg/mL, packaged in a) 1 mL single-dose vial (NDC# 0009-3475-01), b) 25-count box (NDC 0009-3475-03), Rx only, MFG: Pfizer
Check against the official notice below — it lists the full affected range.
McKesson Medical-Surgical Inc. is recalling Depo-Medrol (methylprednisolone acetate injectable suspension, USP) 80mg/mL in 1 mL single-dose vials nationwide due to temperature abuse during handling. The recall affects 177 cartons of the product, and the company was unable to identify specific lot numbers for individual recipients, instead providing distribution dates to customers to help them determine if they received affected product.
The source does not specify a remedy for affected consumers.
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: 177 cartons 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.