Class II · Moderate riskTerminated Initiated Oct 19, 2015 (11 years ago)
Medroxyprogesterone 150/LID 5 mg/mL Injection
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Assurance of Sterility
What was recalled
Medroxyprogesterone 150/LID 5 mg/mL Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
Recalling firm
Western Drug
Origin
AZ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0413-2016
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Reason Severe thunderstorms caused transit delays of certain cold chain products that were shipped on 02-Apr-2025 and delivered after the 48-hours specified delivery time, on 07-Apr-2025 and 08-Apr-2025. The affected products may not have been stored at the recommended labeled storage conditions which may have impacted the safety, quality, identity, potency and purity of the product.
Mckesson Medical-Surgical Inc. Corporate OfficeNDC 55150-0330-01D-0400-2025