Suprax recall
Suprax (cefixime for oral suspension) USP, 100 mg/5 mL, 50 mL bottles (when reconstituted), Manufactured for Lupin Pharmaceuticals, Inc. 111 South…
Why was Suprax recalled?
Discoloration; Product may not meet specifications for color description once reconstituted.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #s: MSA 2021A, MSA 2024A, MSA 2025A, Exp July 2014
- Product
- Suprax (cefixime for oral suspension) USP, 100 mg/5 mL, 50 mL bottles (when reconstituted), Manufactured for Lupin Pharmaceuticals, Inc. 111 South…
- Recalling firm
- Lupin Pharmaceuticals Inc.
- Quantity
- 64,368 bottles
- Distribution
- Nationwide
- Recall date
- April 24, 2013
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)