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Class II: temporary or reversible health riskCompleted

Cardinal Health Trulicity Recall

Trulicity (dulaglutide) injection, 1

Cardinal Health Inc. · Dublin, OH

Risk level
Class II
Reported by FDA
May 25, 2022
Recall ID
D-0883-2022
Check your lot numberHow we source this data

Summary

Cardinal Health recalled Trulicity starting Apr 5, 2022. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0883-2022 on May 25, 2022. Reason: TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions due to inclement weather. Status: Completed.

Why it was recalled

TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions due to inclement weather.

Product description

Trulicity (dulaglutide) injection, 1.5 mg/0.5mL once weekly, 4 Single-Dose Pens, Rx only, Eli Lilly and Company, Indianapolis, IN 46285, NDC 00002-1434-80

Lot numbers, UPCs & expiration codes

Lot #: D482749A, Exp: 10/15/2023.

Where it was sold

NM only

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0883-2022
Classification
Class II
Status
Completed
Recall initiated
Apr 5, 2022
FDA report date
May 25, 2022
Quantity
1 box
Recall type
Voluntary: Firm initiated
Recalling firm
Cardinal Health Inc.

Original FDA data

Every field from FDA enforcement report D-0883-2022, exactly as published.

Show all FDA fields
City
Dublin
State
OH
Status
Completed
Country
United States
Event ID
89976
Address
7000 Cardinal Pl
Code information
Lot #: D482749A, Exp: 10/15/2023.
Postal code
43017-1091
Report date
May 25, 2022
Product type
Drugs
Recall number
D-0883-2022
Classification
Class II
Recalling firm
Cardinal Health Inc.
Product quantity
1 box
Reason for recall
TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions due to inclement weather.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Trulicity (dulaglutide) injection, 1.5 mg/0.5mL once weekly, 4 Single-Dose Pens, Rx only, Eli Lilly and Company, Indianapolis, IN 46285, NDC 00002-1434-80
Distribution pattern
NM only
Recall initiation date
Apr 5, 2022
Initial firm notification
Letter
Center classification date
May 19, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0883-2022, published May 25, 2022. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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