Heparin 12 recall: Sterility Concern
HEPARIN 12,500 Units in 5% Dextrose. (Heparin Sodium, USP 12,500 Units, 5% Dextrose Inj., USP 250 mL) Volume: 252.5 mL. Single dose bag. Avella…
Why was Heparin 12 recalled?
Lack of Assurance of Sterility: Potential leakage of bags.
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 #: 138-20181105@65,138-20181105@64, 138-20181105@63, BUD 8/19/2018.
- Product
- HEPARIN 12,500 Units in 5% Dextrose. (Heparin Sodium, USP 12,500 Units, 5% Dextrose Inj., USP 250 mL) Volume: 252.5 mL. Single dose bag. Avella…
- Recalling firm
- Avella of Deer Valley, Inc. Store 38
- Quantity
- 900 bags
- Distribution
- Nationwide in the USA
- Recall date
- July 25, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)