Cadence Pharmaceuticals recalls OFIRMEV (acetaminophen) injection, 1000 mg/100 mL (10 mg/mL), 24-count Single Use 100 mL Vials per carton, Rx only, Manu
Recalled August 8, 2012 · FDA recall D-1432-2012 · Cadence Pharmaceuticals
Hazard
Presence of Particulate Matter: The firm initiated the recall due to visible presence of particulate matter. · FDA Class II
Units
1,098,912 vials
Sold at
Nationwide
Description
Presence of Particulate Matter: The firm initiated the recall due to visible presence of particulate matter.
Product
OFIRMEV (acetaminophen) injection, 1000 mg/100 mL (10 mg/mL), 24-count Single Use 100 mL Vials per carton, Rx only, Manufactured for: Cadence Pharmaceuticals, Inc., San Diego, CA 92130, NDC 43825-102-01, UPC 3 43825 10201 7.
Manufacturer(s)
Cadence Pharmaceuticals
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →