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Class II: temporary or reversible health riskTerminated

Cardinal Healthcare Lithium Carbonate Extended-Release Tablets Recall

Lithium Carbonate Extended-Release Tablets, USP, 300 mg, 100 Tablets per bottle, Rx onl…

CARDINAL HEALTHCARE · Dublin, OH

Risk level
Class II
Reported by FDA
Jan 3, 2024
Recall ID
D-0189-2024
Check your lot numberHow we source this data

Summary

Cardinal Healthcare recalled Lithium Carbonate Extended-Release Tablets starting Jan 26, 2022. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0189-2024 on Jan 3, 2024. Reason: CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions. Status: Terminated.

Why it was recalled

CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.

Product description

Lithium Carbonate Extended-Release Tablets, USP, 300 mg, 100 Tablets per bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505. NDC: 0378-1300-01

Lot numbers, UPCs & expiration codes

Batch 3138326

Where it was sold

Nationwide USA

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-0189-2024
Classification
Class II
Status
Terminated
Recall initiated
Jan 26, 2022
FDA report date
Jan 3, 2024
Quantity
1 unit
Recall type
Voluntary: Firm initiated
Recalling firm
CARDINAL HEALTHCARE

Original FDA data

Every field from FDA enforcement report D-0189-2024, exactly as published.

Show all FDA fields
City
Dublin
State
OH
Status
Terminated
Country
United States
Event ID
89450
Address
7200 Cardinal Pl W
Code information
Batch 3138326
Postal code
43017-1094
Report date
Jan 3, 2024
Product type
Drugs
Recall number
D-0189-2024
Classification
Class II
Recalling firm
CARDINAL HEALTHCARE
Product quantity
1 unit
Termination date
Sep 29, 2024
Reason for recall
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Lithium Carbonate Extended-Release Tablets, USP, 300 mg, 100 Tablets per bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505. NDC: 0378-1300-01
Distribution pattern
Nationwide USA
Recall initiation date
Jan 26, 2022
Initial firm notification
Letter
Center classification date
Dec 26, 2023

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0189-2024, published Jan 3, 2024. 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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