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Class II: temporary or reversible health riskTerminated

King Legacy, a wholly owned subsidiary of Pfizer Levoxyl Recall

Levoxyl (levothyroxine sodium) tablets, USP, 175 mcg, packaged in a) 100-count bottles…

King Legacy, a wholly owned subsidiary of Pfizer · Bristol, TN

Risk level
Class II
Reported by FDA
May 29, 2013
Recall ID
D-430-2013
Check your lot numberHow we source this data

Summary

King Legacy, a wholly owned subsidiary of Pfizer recalled Levoxyl starting Apr 30, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-430-2013 on May 29, 2013. Reason: Subpotent Drug: The products were below specification for potency at the expiry stability point. Status: Terminated.

Why it was recalled

Subpotent Drug: The products were below specification for potency at the expiry stability point.

Product description

Levoxyl (levothyroxine sodium) tablets, USP, 175 mcg, packaged in a) 100-count bottles (NDC 60793-859-01) and b) 1000-count bottles (NDC 60793-859-10), Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc., Bristol, TN 37620

Lot numbers, UPCs & expiration codes

Lot # a) 64329, Exp. 5/13; 65229, Exp. 6/13; and 65913, Exp. 9/13; b) 64330, Exp. 5/13; 65230, Exp. 6/13; and 65915, Exp. 9/13

Where it was sold

Nationwide and Puerto Rico

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-430-2013
Classification
Class II
Status
Terminated
Recall initiated
Apr 30, 2013
FDA report date
May 29, 2013
Quantity
51,438 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
King Legacy, a wholly owned subsidiary of Pfizer

Original FDA data

Every field from FDA enforcement report D-430-2013, exactly as published.

Show all FDA fields
City
Bristol
State
TN
Status
Terminated
Country
United States
Event ID
65172
Address
501 5th Street
Code information
Lot # a) 64329, Exp. 5/13; 65229, Exp. 6/13; and 65913, Exp. 9/13; b) 64330, Exp. 5/13; 65230, Exp. 6/13; and 65915, Exp. 9/13
Postal code
37620-2304
Report date
May 29, 2013
Product type
Drugs
Recall number
D-430-2013
Classification
Class II
Recalling firm
King Legacy, a wholly owned subsidiary of Pfizer
Product quantity
51,438 bottles
Termination date
Jun 30, 2016
Reason for recall
Subpotent Drug: The products were below specification for potency at the expiry stability point.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Levoxyl (levothyroxine sodium) tablets, USP, 175 mcg, packaged in a) 100-count bottles (NDC 60793-859-01) and b) 1000-count bottles (NDC 60793-859-10), Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc., Bristol, TN 37620
Distribution pattern
Nationwide and Puerto Rico
Recall initiation date
Apr 30, 2013
Initial firm notification
Letter
Center classification date
May 20, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-430-2013, published May 29, 2013. View the source record (openFDA) · FDA enforcement reports

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

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