Linezolid Injection 600 mg/300 mL recall: Particulate Matter
Linezolid Injection 600 mg/300 mL (2 mg/mL), 300 mL Single-use, ready-to-use flexible plastic infusion bags in a foil laminate overwrap, Rx only, Mfd…
Why was Linezolid Injection 600 mg/300 mL recalled?
Presence of Particulate Matter; white particulate matter identified as mold was found in one bag
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 # CLZ160007, Exp August 2018
- Product
- Linezolid Injection 600 mg/300 mL (2 mg/mL), 300 mL Single-use, ready-to-use flexible plastic infusion bags in a foil laminate overwrap, Rx only, Mfd…
- Recalling firm
- AuroMedics Pharma LLC
- Quantity
- 9,050 bags
- Distribution
- Product was distributed throughout United States.
- Recall date
- February 14, 2018
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)