FDAClass IIJune 5, 2019

Cefdinir for Oral Suspension USP recall: Foreign Material

Cefdinir for Oral Suspension USP, 250mg/5mL, Powder for oral suspension, 60 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc.…

Why was Cefdinir for Oral Suspension USP recalled?

Complaint received of metal piece identified in the product bottle prior to the reconstitution.

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 # F802335, exp. date November 2020

Product
Cefdinir for Oral Suspension USP, 250mg/5mL, Powder for oral suspension, 60 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc.…
Recalling firm
Lupin Pharmaceuticals Inc.
Quantity
18,408, 60 mL bottles
Distribution
Distributed Nationwide in the USA
Recall date
June 5, 2019
Classification
Class II
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls