Ascorbic Acid 500 MG/ML Inj., Qty: 50 mL Vial, MFG by: Mylan Institutional, Rockford, IL 61103, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0431-16
Reported: December 16, 2015 Initiated: November 11, 2015 #D-0514-2016
Product Description
Ascorbic Acid 500 MG/ML Inj., Qty: 50 mL Vial, MFG by: Mylan Institutional, Rockford, IL 61103, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0431-16
Reason for Recall
Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Details
- Recalling Firm
- RemedyRepack Inc.
- Units Affected
- 1 Vial
- Distribution
- Nationwide
- Location
- Indiana, PA
Frequently Asked Questions
What product was recalled? ▼
Ascorbic Acid 500 MG/ML Inj., Qty: 50 mL Vial, MFG by: Mylan Institutional, Rockford, IL 61103, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0431-16. Recalled by RemedyRepack Inc.. Units affected: 1 Vial.
Why was this product recalled? ▼
Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on December 16, 2015. Severity: Moderate. Recall number: D-0514-2016.
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