Lupin Pharmaceuticals Inc. recalls Cefdinir for Oral Suspension USP 125 mg/5 mL (60 mL when reconstituted), 60 mL bottle, Rx only, Manufactured for: Lupin
Recalled May 22, 2024 · FDA recall D-0497-2024 · Lupin Pharmaceuticals
Hazard
Presence of foreign substance: Product complaint of foreign material in reconstituted bottle. · FDA Class II
Units
17,040 bottles
Sold at
USA nationwide
Description
Presence of foreign substance: Product complaint of foreign material in reconstituted bottle.
Product
Cefdinir for Oral Suspension USP 125 mg/5 mL (60 mL when reconstituted), 60 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, United States, Manufactured by: Lupin Limited, Mandideep 462 046, India, NDC 68180-722-04
Manufacturer(s)
Lupin Pharmaceuticals Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →