FDA recall record

Cubist Pharmaceuticals CUBICIN (daptomycin for injection), 500 mg single-use vial recall — FDA D-1382-2014

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

Class Iclassification
D-1382-2014official record ID
Jun 18, 2014report date

Recall record at a glance

Official recordD-1382-2014
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmCubist Pharmaceuticals, Inc.
Report dateJun 18, 2014
Recall initiation dateApr 17, 2014
Quantity51,500 vials
LocationLexington, MA, United States

Official product description

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.

Why the product was recalled

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

Distribution information

Nationwide and Puerto Rico.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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