Cefuroxime 10 mg/mL in Sodium Chloride recall
Cefuroxime 10 mg/mL in Sodium Chloride, Intravitreal injection, 1 mL in a 2mL Vial, Ophthalmic Use Only, Office Use Only, Leiter's (800) 292-6772- 17…
Why was Cefuroxime 10 mg/mL in Sodium Chloride recalled?
Incorrect Product Formulation; compounded sterile drug reconstituted using sterile water instead of sterile 0.9% Sodium Chloride.
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 # 1811195, Exp. Date: 05/01/19
- Product
- Cefuroxime 10 mg/mL in Sodium Chloride, Intravitreal injection, 1 mL in a 2mL Vial, Ophthalmic Use Only, Office Use Only, Leiter's (800) 292-6772- 17…
- Recalling firm
- Leiter's Enterprises, Inc.
- Quantity
- 569 vials
- Distribution
- CA, AZ, MI, NY
- Recall date
- March 13, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)