Rocuronium Bromide in all strengths, all doses, and all packaging.
FDA Recall #D-0467-2018 — Class II — December 27, 2017
Product Description
Rocuronium Bromide in all strengths, all doses, and all packaging.
Reason for Recall
Lack of sterility assurance.
Recalling Firm
Pharmedium Services, LLC — Lake Forest, IL
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Drugs
Product Quantity
Unknown
Distribution
U.S.A. Nationwide
Code Information
All lots remaining within expiry.
Status
Terminated
Voluntary / Mandated
Voluntary: Firm initiated