# FDA recall D-0511-2016

> **RemedyRepack Inc.** · Class II · drug recall initiated 2015-11-11.

## Product

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.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0511-2016
- **Recalling firm:** RemedyRepack Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-11-11
- **Report date:** 2015-12-16
- **Termination date:** 2016-11-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Indiana, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0511-2016

## Citation

> AI Analytics. FDA recall D-0511-2016. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-0511-2016. Source: US FDA. Licensed CC0.

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