Cefdinir for Oral Suspension USP, 250 mg/5 mL, packaged in a 60 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202, Manufactured by: Lupin Limited, Mandideep, 462 046 India, NDC 68180-723-04
Reported: June 5, 2024 Initiated: May 8, 2024 #D-0518-2024
Product Description
Cefdinir for Oral Suspension USP, 250 mg/5 mL, packaged in a 60 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202, Manufactured by: Lupin Limited, Mandideep, 462 046 India, NDC 68180-723-04
Reason for Recall
Defective container: lack of seal integrity.
Details
- Recalling Firm
- Lupin Pharmaceuticals Inc.
- Units Affected
- 51,006 bottles
- Distribution
- USA Nationwide
- Location
- Baltimore, MD
Frequently Asked Questions
What product was recalled? ▼
Cefdinir for Oral Suspension USP, 250 mg/5 mL, packaged in a 60 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202, Manufactured by: Lupin Limited, Mandideep, 462 046 India, NDC 68180-723-04. Recalled by Lupin Pharmaceuticals Inc.. Units affected: 51,006 bottles.
Why was this product recalled? ▼
Defective container: lack of seal integrity.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 5, 2024. Severity: Moderate. Recall number: D-0518-2024.
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