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
Reported: November 13, 2019 Initiated: November 1, 2019 #D-0305-2020
Product Description
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
Reason for Recall
Presence of Foreign substance: identified as a dead ant.
Details
- Recalling Firm
- Lupin Pharmaceuticals Inc.
- Units Affected
- 30,516 bottles
- Distribution
- Product was distributed to major distributors/wholesalers throughout the United States.
- Location
- Baltimore, MD
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Lupin Pharmaceuticals Inc.. Units affected: 30,516 bottles.
Why was this product recalled? ▼
Presence of Foreign substance: identified as a dead ant.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 13, 2019. Severity: Low. Recall number: D-0305-2020.
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