Right Value Drug Stores Tadalafil SR 12mg Capsules Misbranded
Right Value Drug Stores recalls Tadalafil SR 12mg capsules with specific bottle sizes and lots due to misbranding. Consumers should check labels for NDC 99999-9969-51 and affected lots.
Lower-risk recall
Labeling Not Elsewhere Classified: Misbranding.
Contact the company
What happened, in plain English
Right Value Drug Stores is recalling Tadalafil SR 12mg capsules in specific bottle sizes sold through Carie Boyd's Prescription Shop. The recall is for misbranding, meaning the product labels don't match the actual contents. Read more at govinfonow.com/recall/39549-right-value-drug-stores-tadalafil-sr-12mg-capsules-misbranded.
Source Summary by GovInfoNow · govinfonow.com/recall/39549-right-value-drug-stores-tadalafil-sr-12mg-capsules-misbranded · Updated October 6, 2026 · FDA enforcement record: FDA #D-0243-2019
Cite this page
“Right Value Drug Stores Tadalafil SR 12mg Capsules Misbranded.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/39549-right-value-drug-stores-tadalafil-sr-12mg-capsules-misbranded. Based on FDA recall #D-0243-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0243-2019%22&limit=1).
Why it’s dangerous
The product is misbranded, meaning the labeling does not correctly describe the product. This could lead to confusion about the medication's strength or content, but it does not pose a direct health risk.
Who’s affected
People who purchased Tadalafil SR 12mg capsules from Carie Boyd's Prescription Shop in Hurst, Texas, with the listed NDC and lots. Those most at risk are individuals using the medication for erectile dysfunction.
How to tell if you have this one
Check for Tadalafil SR 12mg capsules in 8, 13, 20, 30, 40, or 60 dram screw top bottles. Look for NDC 99999-9969-51 and lots 07232018@15 (expiring 1/19/2019) or 08102018@10 (expiring 2/6/2019).
- Brand
Right Value Drug Stores- Category
Drug
All 4 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class III- Status
Terminated- Distribution
Distributed in California
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0240-2019 | Progesterone SR 100 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 99999-0104-55; Lots: 03272018@10 Exp. 09/11/2018; 03282018@8 Exp. 09/24/2018; 03282018@18 Exp. 09/24/2018; 04232018@3 Exp. 09/24/2018; 05302018@4 Exp. 10/22/2018; 06072018@6 Exp. 10/22/2018; 06212018@1 Exp. 10/22/2018; 06252018@7 Exp. 10/22/2018; 07192018@8 Exp. 10/22/2018; 07192018@10 Exp. 01/15/2019; 08282018@6 Exp. 2/23/2019; 08282018@7 Exp. 2/23/2019; 09142018@1 Exp. 02/23/2018; 09182018@10 Exp. 2/23/2019 | 6580 capsules |
| D-0241-2019 | 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; 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 | 8240 capsules |
| D-0242-2019 | Tadalafil SR 7 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. NDC 99999-9970-88; Lots: 04242018@16 Exp. 10/21/2018; 05042018@17 Exp. 10/31/2018; 07232018@13 Exp. 01/19/2019; 08032018@2 Exp. 01/30/2019 | 660 capsules |
| D-0243-2019 | Tadalafil SR 12 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 99999-9969-51; Lots: 07232018@15 Exp. 1/19/2019; 08102018@10 Exp. 2/6/2019 | 180 capsules |
What to do — step by step
Check Product Label
Look for NDC 99999-9969-51 and the specific lots listed in the recall.
Where it went and when
Where it was distributed
Distributed in California.
FDA distribution: “Distributed in California” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California.
Recall timeline
FDA terminated this recall 2.1 years after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Is this product dangerous?
No, the recall is for misbranding, not a safety hazard. The product is safe to use but needs correct labeling.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0243-2019 (September 25, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0243-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.