oxyTOCIN 30 Units/500 mL recall
oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride, Injection for IV Use, High Alert, This is a Compounded Product for…
Why was oxyTOCIN 30 Units/500 mL recalled?
Incorrect Product Formulation: Oxytocin 30 units was added to an IV bag of 0.45% Sodium Chloride (500mL) instead of 0.9% Sodium Chloride (500mL).
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 30027403, BUD 11/14/2022
- Product
- oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride, Injection for IV Use, High Alert, This is a Compounded Product for…
- Recalling firm
- QuVa Pharma, Inc.
- Quantity
- 1994 bags
- Distribution
- Nationwide in the USA
- Recall date
- October 5, 2022
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)