CLASS II Drug recall · Reported 2 Jun 2021 · FDA Enforcement Report

Tramadol Hydrochloride Tablets USP 100mg recalled by Cardinal Health

Cardinal Health is recalling Tramadol Hydrochloride Tablets USP 100mg, distributed in Florida, Georgia, South Carolina. The recall was initiated on 15 Mar 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes200340H1
Quantity recalled86 BOTTLE

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-0586-2021
FDA event ID
87512
Recalling firm
Cardinal Health, Dublin, OH
Classification
Class II
Status
Terminated
Recall initiated
15 Mar 2021
FDA classified
24 May 2021
Reported
2 Jun 2021
Type
Voluntary: Firm initiated
Customers notified by
Letter
Drug class
Pain Medication

Timeline

15 Mar 2021Recall initiated by company
24 May 2021Classified by FDA+70 days
2 Jun 2021Published 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: Intermittent exposure to temperature excursion during storage.

Product as listed by the FDA

TRAMADOL HYDROCHLORIDE TABLETS USP 100MG, 100-count bottle, Rx Only, Manufactured by: Rubicon Research :Private Limited, Ambernath, Dist. Thane, 421506 India, NDC: 52817-0196-10

Where it was distributed

FL, GA, SC

FloridaGeorgiaSouth Carolina

Questions about this recall

Is Tramadol Hydrochloride Tablets USP 100mg recalled?

Yes. Cardinal Health recalled Tramadol Hydrochloride Tablets USP 100mg on 15 Mar 2021. The recall is Class II and its status is Terminated. Recall number D-0586-2021.

Why was it recalled?

CGMP Deviations: Intermittent exposure to temperature excursion during storage.

Which lots are affected?

200340H1

Where was it sold?

FL, GA, SC

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

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