# FDA recall D-0723-2026

> **Lupin Pharmaceuticals Inc.** · Class II · drug recall initiated 2026-06-23.

## Product

Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection USP, 1mg per vial, Diluent for Glucagon, 1 mL syringe, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL 34108, Manufactured by: Lupin Limited, Nagpur - 441108, INDIA, NDC 70748-311-01

## Reason for recall

CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.

## Distribution

Nationwide within the U.S.

## Key facts

- **Recall number:** D-0723-2026
- **Recalling firm:** Lupin Pharmaceuticals Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2026-06-23
- **Report date:** 2026-07-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Naples, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0723-2026

## Citation

> AI Analytics. FDA recall D-0723-2026. Retrieved 2026-09-01 from https://api.ai-analytics.org/recall/D-0723-2026. Source: US FDA. Licensed CC0.

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