FDA Drug Recalls

Recalls / Class II

Class IID-0513-2016

Product

Vitamin B-Complex 100, Multi MG Inj, Qty: 30 mL Vial, MFG by: Mylan Institutional, Rockford, IL 61103, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 52125-0873-02

Affected lot / code info
Lot # B0105037-100715, Exp 10/01/2016

Why it was recalled

Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.

Recalling firm

Firm
RemedyRepack Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
625 Kolter Dr Ste 4, N/A, Indiana, Pennsylvania 15701-3571

Distribution

Quantity
1 Vial
Distribution pattern
Nationwide

Timeline

Recall initiated
2015-11-11
FDA classified
2015-12-04
Posted by FDA
2015-12-16
Terminated
2016-11-01
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0513-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.