CLASS III Drug recall · Reported 5 Sep 2018 · FDA Enforcement Report

Calcitriol Oral Solution, 1 mcg/mL recalled by Validus Pharmaceuticals

Validus Pharmaceuticals is recalling Calcitriol Oral Solution, 1 mcg/mL, distributed nationwide in the US. The recall was initiated on 15 Jun 2018 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesRV1602RB, Exp 07/2019; RV1604RB, Exp 9/2019; RV1605RB, Exp 10/2019
Quantity recalled7864 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-1170-2018
FDA event ID
80326
Recalling firm
Validus Pharmaceuticals, Parsippany, NJ
Classification
Class III
Status
Terminated
Recall initiated
15 Jun 2018
FDA classified
5 Sep 2018
Reported
5 Sep 2018
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

15 Jun 2018Recall initiated by company
5 Sep 2018Classified by FDA+82 days
5 Sep 2018Published in enforcement report+0 days

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

Reason for recall

Subpotency: lower than expected potency result was obtained at the 18 month stability time point.

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

Calcitriol Oral Solution, 1 mcg/mL, 15 mL bottle, Rx Only, Distributed by: Ranbaxy Pharmaceuticals Inc. Jacksonville, FL 32257 USA, NDC 63304-241-59

Where it was distributed

U.S. nationwide

Nationwide

Questions about this recall

Is Calcitriol Oral Solution, 1 mcg/mL recalled?

Yes. Validus Pharmaceuticals recalled Calcitriol Oral Solution, 1 mcg/mL on 15 Jun 2018. The recall is Class III and its status is Terminated. Recall number D-1170-2018.

Why was it recalled?

Subpotency: lower than expected potency result was obtained at the 18 month stability time point.

Which lots are affected?

RV1602RB, Exp 07/2019; RV1604RB, Exp 9/2019; RV1605RB, Exp 10/2019

Where was it sold?

U.S. 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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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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