PlainRecalls
FDA Drug Moderate Class II Terminated

Humulin 70/30, 100 Units/mL Inj, Qty: 10 mL Vial, MFG by: Lilly USA, LLC, Indianapolis, IN 46285, Repackaged by: Remedy Repack, Inc, 625 Kolter Dr, Indiana, PA 15701, NDC 52125-0415-08

Reported: December 16, 2015 Initiated: November 11, 2015 #D-0511-2016

Product Description

Humulin 70/30, 100 Units/mL Inj, Qty: 10 mL Vial, MFG by: Lilly USA, LLC, Indianapolis, IN 46285, Repackaged by: Remedy Repack, Inc, 625 Kolter Dr, Indiana, PA 15701, NDC 52125-0415-08

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
65 Vials
Distribution
Nationwide
Location
Indiana, PA

Frequently Asked Questions

What product was recalled?
Humulin 70/30, 100 Units/mL Inj, Qty: 10 mL Vial, MFG by: Lilly USA, LLC, Indianapolis, IN 46285, Repackaged by: Remedy Repack, Inc, 625 Kolter Dr, Indiana, PA 15701, NDC 52125-0415-08. Recalled by RemedyRepack Inc.. Units affected: 65 Vials.
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-0511-2016.