D-0668-2016 Class I Terminated
FDA drug recall D-0668-2016 was initiated by Hospira Inc. on January 5, 2016 and is designated Class I. Reason for recall: Labeling: Incorrect Barcode: Primary bag labeling may be mislabeled with the wrong barcode which scans in as heparin sodium. The recall status is terminated (terminated September 28, 2017). Affected quantity: 213,600 bags.
Recall Details
- Product Type
- Drugs
- Report Date
- February 24, 2016
- Initiation Date
- January 5, 2016
- Termination Date
- September 28, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 213,600 bags
Product Description
Magnesium Sulfate in Water for Injection, (0.325 mEq Mg++/mL) 40 mg/mL, 2 g Total, 50 mL Single-Dose Container bag, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-6729-24.
Reason for Recall
Labeling: Incorrect Barcode: Primary bag labeling may be mislabeled with the wrong barcode which scans in as heparin sodium.
Distribution Pattern
Nationwide
Code Information
Lot: 53-113-JT, Exp 1NOV2016