US Drug Recall Register
Class I · High risk Terminated Initiated Apr 17, 2014 (12 years ago)

CUBICIN (daptomycin for injection), 500 mg single-use vial, Rx only, Manufactured for…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Presence of Particulate Matter: Customer complaint stating that one vial contained a glass shard.

What was recalled

CUBICIN (daptomycin for injection), 500 mg single-use vial, Rx only, Manufactured for: Cubist Pharmaceuticals, Inc., Lexington, MA 02421, NDC 67919-011-01, UPC 3 67919-011-01 6.

Recalling firm
Cubist Pharmaceuticals, Inc.
NDC code
67919-011-01
Origin
MA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1382-2014

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.

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