FDAClass IJune 18, 2014

Cubicin recall: Particulate Matter

CUBICIN (daptomycin for injection), 500 mg single-use vial, Rx only, Manufactured for: Cubist Pharmaceuticals, Inc., Lexington, MA 02421, NDC…

Why was Cubicin recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot #: 280453F, Exp 04/16

Product
CUBICIN (daptomycin for injection), 500 mg single-use vial, Rx only, Manufactured for: Cubist Pharmaceuticals, Inc., Lexington, MA 02421, NDC…
Recalling firm
Cubist Pharmaceuticals, Inc.
Quantity
51,500 vials
Distribution
Nationwide and Puerto Rico.
Recall date
June 18, 2014
Classification
Class I
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls