Deferoxamine 3300 mg/20 mL Sterile Water for Injection recall: Sterility Concern
Deferoxamine 3300 mg/20 mL Sterile Water for Injection syringe, FOR SUBCUTANEOUS USE ONLY, Baptist Health Medical Towers Pharmacy & Infusion, Little…
Why was Deferoxamine 3300 mg/20 mL Sterile Water for Injection recalled?
Lack of Sterility Assurance
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?
All product remaining within expiry
- Product
- Deferoxamine 3300 mg/20 mL Sterile Water for Injection syringe, FOR SUBCUTANEOUS USE ONLY, Baptist Health Medical Towers Pharmacy & Infusion, Little…
- Recalling firm
- Baptist Health Medical Towers Pharmacy and Infusion Services
- Quantity
- 5 bags
- Distribution
- Arkansas
- Recall date
- June 8, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)