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Class II · ModerateRecall completed

Alprazolam

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot EJ9591
Where it was soldNationwide
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 Substance; tablets may contain stainless steel metal particulates

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 bySandoz Inc
Brand nameALPRAZOLAM
Generic nameALPRAZOLAM
Active ingredient(s)ALPRAZOLAM
Distributed by / forSandoz Incorporated
NDC0781-1061-10
Show the full FDA record
Full product labelAlprazolam Tablets, USP, 0.25mg, Rx only, 1000 tablets, Sandoz Inc., Princeton, NJ --- NDC 0781-1061-10
Recalling firmSandoz Incorporated
DistributionNationwide
Quantity1,332 bottles
Recall initiated2014-07-25
Report date2014-08-06
Recall completed2015-02-05
Recall numberD-1509-2014
ClassificationClass II
FDA statusTerminated
Origin on fileBroomfield CO United States

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.