Lupin Pharmaceuticals Inc. recalls Cefdinir for Oral Suspension USP, 250 mg/5mL,100 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Balt
Recalled November 13, 2019 · FDA recall D-0305-2020 · Lupin Pharmaceuticals
Hazard
Presence of Foreign substance: identified as a dead ant. · FDA Class III
Units
30,516 bottles
Sold at
Product was distributed to major distributors/wholesalers throughout the United States.
Description
Presence of Foreign substance: identified as a dead ant.
Product
Cefdinir for Oral Suspension USP, 250 mg/5mL,100 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, United States, Manufactured by: Lupin Limited, Mandideep 462 046 INDIA, NDC 68180-723-10
Manufacturer(s)
Lupin Pharmaceuticals Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →