CLASS III Drug recall · Reported 21 Nov 2018 · FDA Enforcement Report

Progesterone SR recalled by Right Value Drug Stores

Right Value Drug Stores is recalling Progesterone SR, distributed in California. The recall was initiated on 25 Sep 2018 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLots: 04052018@16 Exp. 9/11/2018; 04242018@2 Exp. 10/21/2018; 05072018@8 Exp. 10/21/2018; 05302018@3 Exp. 10/22/2018; 06192018@9 Exp. 10/22/2018; 06192018@10 Exp. 12/15/2018; 06202018@12 Exp. 12/15/2018; 07022018@15 Exp. 12/15/2018; 07242018@2 Exp. 1/13/2018; 08312018@3 Exp. 2/6/2018
Quantity recalled8240 capsules

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-0241-2019
FDA event ID
81198
Recalling firm
Right Value Drug Stores, Hurst, TX
Classification
Class III
Status
Terminated
Recall initiated
25 Sep 2018
FDA classified
14 Nov 2018
Reported
21 Nov 2018
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Labeling Errors

Timeline

25 Sep 2018Recall initiated by company
14 Nov 2018Classified by FDA+50 days
21 Nov 2018Published in enforcement report+7 days

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

Reason for recall

Labeling Not Elsewhere Classified: Misbranding.

Product as listed by the FDA

Progesterone SR 200 mg Capsules, packed in 8,13, 20, 30, 40 or 60 dram screw top pill bottle, Carie Boyd's Prescription Shop 122 Grapevine Hwy. Hurst, TX 76054 817-282-9376. NDC 99999-0018-74

Where it was distributed

Distributed in California

California

Questions about this recall

Is Progesterone SR recalled?

Yes. Right Value Drug Stores recalled Progesterone SR on 25 Sep 2018. The recall is Class III and its status is Terminated. Recall number D-0241-2019.

Why was it recalled?

Labeling Not Elsewhere Classified: Misbranding.

Which lots are affected?

Lots: 04052018@16 Exp. 9/11/2018; 04242018@2 Exp. 10/21/2018; 05072018@8 Exp. 10/21/2018; 05302018@3 Exp. 10/22/2018; 06192018@9 Exp. 10/22/2018; 06192018@10 Exp. 12/15/2018; 06202018@12 Exp. 12/15/2018; 07022018@15 Exp. 12/15/2018; 07242018@2 Exp. 1/13/2018; 08312018@3 Exp. 2/6/2018

Where was it sold?

Distributed in California

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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