Dextrose Injection recall: Particulate Matter
Dextrose Injection,USP,70% 2000 mL VIAFLEX Plastic Container Bag, Pharmacy Bulk Package, Not For Direct Infusion, Must Be Diluted, Rx Only…
Why was Dextrose Injection recalled?
Presence of Particulate Matter: Confirmed customer compliants of finding an insect floating in the primary container of each product.
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 # C985150; Exp. 07/16
- Product
- Dextrose Injection,USP,70% 2000 mL VIAFLEX Plastic Container Bag, Pharmacy Bulk Package, Not For Direct Infusion, Must Be Diluted, Rx Only…
- Recalling firm
- Baxter Healthcare Corp.
- Quantity
- 28,080 VIAFLEX Plastic Containers
- Distribution
- Nationwide
- Recall date
- June 15, 2016
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)