---
title: "Trulicity (dulaglutide) injection, 0.75 mg/0.5mL once weekly, 4 Single-Dose P... — FDA record D-0884-2022 | Is It on Recall"
description: "TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions"
url: https://isitonrecall.com/recall/fda-drug-d-0884-2022-trulicity-dulaglutide-injection-0-75-mg-0-5ml-once-weekly-4-single-dose-pens-rx-only-eli-lilly-and-c/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA drug enforcement

# Trulicity (dulaglutide) injection, 0.75 mg/0.5mL once weekly, 4 Single-Dose Pens, Rx only, Eli Lilly and Company, Ind... — FDA record D-0884-2022

Reported completed

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 5, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Trulicity (dulaglutide) injection, 0.75 mg/0.5mL once weekly, 4 Single-Dose Pens, Rx only, Eli Lilly and Company, Indianapolis, IN 46285, NDC 0002-1433-80
- **Reason**: TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions
- **Classification**: Class II
- **Recalling firm**: Cardinal Health Inc.
- **Quantity**: 1 box
- **Agency-reported status**: Completed
- **Source record identifier**: D-0884-2022

[Open the official record](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0884-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot #: D484557A, Exp: 10/25/2023. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

NM only

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [New Mexico](https://isitonrecall.com/state/new-mexico/)

## Dates in the source

- **Report date**: May 25, 2022
- **Recall initiation date**: Apr 5, 2022
- **Center classification date**: May 19, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0884-2022%22)

## Before changing a medicine

Follow urgent instructions in the current official recall notice. Speak to your pharmacist or prescriber before stopping or changing a prescribed medicine.

Talk to your doctor or pharmacist if you have questions or concerns about your medicine. [FDA medication recall guidance](https://www.fda.gov/drugs/drug-recalls/understanding-drug-recalls-what-know-and-what-do)

## Related records

[Medications records](https://isitonrecall.com/category/medications/) [Cardinal Health Inc. records](https://isitonrecall.com/brand/cardinal-health-inc/)