CLASS II Drug recall · Reported 8 Mar 2023 · FDA Enforcement Report

rOPINIRole Tablets USP 5 mg* recalled by Accord Healthcare

Accord Healthcare is recalling rOPINIRole Tablets USP 5 mg*, distributed in Puerto Rico. The recall was initiated on 7 Feb 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBatches: P2104150, P2104151, Exp. Date 6/30/2023, P2202065, Exp. Date 3/31/2024
NDC16729-232, 16729-233, 16729-234, 16729-235, 16729-236, 16729-237
UPC316729238014
Quantity recalled5,112 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-0431-2023
FDA event ID
91657
Recalling firm
Accord Healthcare, Durham, NC
Manufacturer
Accord Healthcare Inc.
Classification
Class II
Status
Terminated
Recall initiated
7 Feb 2023
FDA classified
2 Mar 2023
Reported
8 Mar 2023
Type
Voluntary: Firm initiated
Customers notified by
Letter

Timeline

7 Feb 2023Recall initiated by company
2 Mar 2023Classified by FDA+23 days
8 Mar 2023Published in enforcement report+6 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: recalling drug products following an FDA inspection.

Product as listed by the FDA

rOPINIRole Tablets USP 5 mg* 100-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703 Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad-382 213 INDIA, NDC 16729-238-01, UPC 3 16729 23801 4

Where it was distributed

United States including Puerto Rico and Canada

Puerto Rico

Questions about this recall

Is rOPINIRole Tablets USP 5 mg* recalled?

Yes. Accord Healthcare recalled rOPINIRole Tablets USP 5 mg* on 7 Feb 2023. The recall is Class II and its status is Terminated. Recall number D-0431-2023.

Why was it recalled?

CGMP Deviations: recalling drug products following an FDA inspection.

Which lots are affected?

Batches: P2104150, P2104151, Exp. Date 6/30/2023, P2202065, Exp. Date 3/31/2024

Where was it sold?

United States including Puerto Rico and Canada

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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