CLASS II Drug recall · Reported 21 May 2014 · FDA Enforcement Report

Indomethacin Capsules USP, 25 mg recalled by Teva Pharmaceuticals U

Teva Pharmaceuticals USA is recalling Indomethacin Capsules USP, 25 mg, distributed nationwide in the US. The recall was initiated on 24 Mar 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesTE32134, Exp. 02/15
Quantity recalled7,694 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-1294-2014
FDA event ID
67811
Recalling firm
Teva Pharmaceuticals USA, Horsham, PA
Classification
Class II
Status
Terminated
Recall initiated
24 Mar 2014
FDA classified
12 May 2014
Reported
21 May 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter

Timeline

24 Mar 2014Recall initiated by company
12 May 2014Classified by FDA+49 days
21 May 2014Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

CGMP Deviations; laboratory testing was not followed in accordance with GMP requirements

Product as listed by the FDA

INDOMETHACIN Capsules USP, 25 mg 100 count bottle, Rx only , Manufactured In INDIA By: EMCURE PHARMACEUTICALS LTD harmaceuticals Ltd., Hinjwadi, Pune, India, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960, NDC 0093-4029-01

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it recalled?

CGMP Deviations; laboratory testing was not followed in accordance with GMP requirements

Which lots are affected?

TE32134, Exp. 02/15

Where was it sold?

Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 67811

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