FDA Recall Reports for Cubicin 500 mg IV – RES #88867/D-0093-2022

FDA Recall Reports for Cubicin 500 mg IV – RES #88867/D-0093-2022

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Original Request Contents: Copies of recall reports for RES #88867 for Cubicin (daptomycin for injection) 500 mg IV, Lot 934778, expiring June 2022; recalling firm Merck Sharp & Dohme Corp; recall number D-0093-2022; NDC: 67919-011-01; trace lot origins
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.

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