Drug recall
CUBICIN (daptomycin for injection), 500 mg single-use vial, Rx only, Manufactured for: Cubist Pharmaceuticals…
FDA recall event 68025 · Class I · Cubist Pharmaceuticals, Inc.
Key facts
| Event ID | 68025 |
|---|---|
| Recall numbers | D-1382-2014 |
| Recalling firm | Cubist Pharmaceuticals, Inc. |
| Product type | Drugs |
| Products | 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. |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Presence of Particulate Matter: Customer complaint stating that one vial contained a glass shard. |
| Initiation date | Apr 17, 2014 |
| Report date | Jun 18, 2014 |
| Termination date | Jul 22, 2016 |
| City | Lexington |
| State | MA |
| Country | United States |
| FEI number | 1000513172 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: