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Class III · Lower riskRecall completed

Fenofibrate

Unlikely to cause harm — often a labeling or packaging issue.

Does this affect you?
Check your lot numberLot #: E181370, Exp. 5/2020
Where it was soldIndiana and Louisiana
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Presence of Foreign Tablet/Capsule: A foreign identified as Valacyclovir tablet 500 mg was co-mingled in a bottle containing Fenofibrate Tablets, USP 145 mg.

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byCamber Pharmaceuticals, Inc.
Brand nameFENOFIBRATE
Generic nameFENOFIBRATE
Active ingredient(s)FENOFIBRATE
Distributed by / forCamber Pharmaceuticals, Inc. Piscataway, NJ, 08854
NDC31722-596-90
Show the full FDA record
Full product labelFenofibrate Tablets, USP 145 mg, 90-count bottles, Rx only, Manufactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ, 08854, NDC 31722-596-90
Recalling firmHetero Labs, Ltd. - Unit III
DistributionIndiana and Louisiana
Quantity5,424 bottles
Recall initiated2018-09-12
Report date2018-10-03
Recall completed2018-11-29
Recall numberD-1211-2018
ClassificationClass III
FDA statusTerminated
Origin on fileHyderabad India

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.