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Class II: temporary or reversible health riskTerminated

Teva Pharmaceuticals Fortamet Recall

Fortamet (metformin HCl) extended release tablets, 1000 mg, 60-count bottle, Rx only, M…

Teva Pharmaceuticals USA · North Wales, PA

Risk level
Class II
Reported by FDA
Oct 31, 2018
Recall ID
D-0098-2019
Check your lot numberHow we source this data

Summary

Teva Pharmaceuticals recalled Fortamet starting Aug 6, 2018. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0098-2019 on Oct 31, 2018. Reason: Defective Delivery System: There is a potential for some tablets to be missing the laser drilling which might affect drug release. Status: Terminated.

Why it was recalled

Defective Delivery System: There is a potential for some tablets to be missing the laser drilling which might affect drug release.

Product description

Fortamet (metformin HCl) extended release tablets, 1000 mg, 60-count bottle, Rx only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314, Distributed by: Shionogi Inc., Florham Park, NJ 07932, NDC 59630-575-60

Lot numbers, UPCs & expiration codes

Lot #: 1237868A, 1248900A, Exp 5/2020

Where it was sold

Product was distributed throughout the United States. Bulk product was distributed to Takeda, Deerfield, IL and may have been further distributed.

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-0098-2019
Classification
Class II
Status
Terminated
Recall initiated
Aug 6, 2018
FDA report date
Oct 31, 2018
Quantity
13,225 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Teva Pharmaceuticals USA

Original FDA data

Every field from FDA enforcement report D-0098-2019, exactly as published.

Show all FDA fields
City
North Wales
State
PA
Status
Terminated
Country
United States
Event ID
80790
Address
1090 Horsham Rd
Code information
Lot #: 1237868A, 1248900A, Exp 5/2020
Postal code
19454-1505
Report date
Oct 31, 2018
Product type
Drugs
Recall number
D-0098-2019
Classification
Class II
Recalling firm
Teva Pharmaceuticals USA
Product quantity
13,225 bottles
Termination date
Feb 13, 2020
Reason for recall
Defective Delivery System: There is a potential for some tablets to be missing the laser drilling which might affect drug release.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Fortamet (metformin HCl) extended release tablets, 1000 mg, 60-count bottle, Rx only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314, Distributed by: Shionogi Inc., Florham Park, NJ 07932, NDC 59630-575-60
Distribution pattern
Product was distributed throughout the United States. Bulk product was distributed to Takeda, Deerfield, IL and may have been further distributed.
Recall initiation date
Aug 6, 2018
Initial firm notification
Letter
Center classification date
Oct 25, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0098-2019, published Oct 31, 2018. 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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