Cefuroxime recall: Subpotent
Cefuroxime, Ophthalmic Solution for Injection, 10 mg/mL, 0.3 mL single-use syringe. This is a Compounded Drug, Hospital & Office Use Only, Not for…
Why was Cefuroxime recalled?
Subpotent Drug: The product is sub-potent prior to its 90-day beyond use date.
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 #: C274-000002725, BUD 1/21/2018; C274-000002790, BUD 1/28/2018; C274-000002989, BUD 2/13/2018; C274-000003008, BUD 2/14/2018; C274-000003077, BUD 2/20/2018
- Product
- Cefuroxime, Ophthalmic Solution for Injection, 10 mg/mL, 0.3 mL single-use syringe. This is a Compounded Drug, Hospital & Office Use Only, Not for…
- Recalling firm
- JCB Laboratories LLC
- Quantity
- 6,510 syriges
- Distribution
- Nationwide within USA
- Recall date
- February 7, 2018
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)