Class II · Moderate riskTerminated Initiated May 17, 2016 (10 years ago)
17-0H PROGESTERONE 250MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding…
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
What was recalled
17-0H PROGESTERONE 250MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Recalling firm
Well Care Compounding Pharmacy
Origin
NV, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0978-2016
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…
Mckesson Medical-Surgical Inc. Corporate OfficeNDC 55150-0330-01D-0400-2025