Accord Healthcare, Inc. recalls Hydrochlorothiazide Tablets USP, 12.5 mg, 100-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Durham,
Accord Healthcare recalls 100-count Hydrochlorothiazide tablets after customer complaints of containing Spironolactone instead. This mix-up could lead to incorrect medication use. Check your prescription bottle for the label and contact your pharmacy.
Lower-risk recall
Product Mix-Up: customer complaint that a sealed bottle labeled as Hydrochlorothiazide Tablets USP 12.5 mg contained only Spironolactone Tablets USP 25 mg.
Contact the company & request your remedy
What happened, in plain English
Accord Healthcare is recalling 100-count Hydrochlorothiazide tablets (12.5 mg) because some bottles were mistakenly labeled as Hydrochlorothiazide but contained Spironolactone tablets. This mix-up could cause incorrect medication use if taken without knowing the actual contents. Read more at govinfonow.com/recall/39696-accord-healthcare-recalls-hydrochlorothiazide-tablets-due-to-mix-up-with.
Source Summary by GovInfoNow · govinfonow.com/recall/39696-accord-healthcare-recalls-hydrochlorothiazide-tablets-due-to-mix-up-with · Updated October 6, 2026 · FDA enforcement record: FDA #D-1206-2018
Cite this page
“Accord Healthcare recalls Hydrochlorothiazide tablets due to mix-up with Spironolactone.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/39696-accord-healthcare-recalls-hydrochlorothiazide-tablets-due-to-mix-up-with. Based on FDA recall #D-1206-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1206-2018%22&limit=1).
Why it’s dangerous
The product was mislabeled, meaning some bottles that were supposed to contain Hydrochlorothiazide tablets actually contained Spironolactone tablets. This mix-up could lead to taking the wrong medication if the patient doesn't notice the incorrect contents.
Who’s affected
People who have a prescription for Hydrochlorothiazide tablets from this manufacturer are affected. Those who have taken the tablets without realizing the mix-up are at risk of incorrect medication use.
How to tell if you have this one
Check if your bottle has the label 'Hydrochlorothiazide Tablets USP 12.5 mg' but contains Spironolactone tablets. The product was sold with NDC 16729-182-01 and lot number PW05264.
- Brand
Accord Healthcare- Category
Drug
What to do — step by step
Check Your Bottle
Look for the label 'Hydrochlorothiazide Tablets USP 12.5 mg' on the bottle but verify the contents match the label.
Questions people ask
Why was this product recalled?
The recall is due to customer complaints that some sealed bottles labeled as Hydrochlorothiazide Tablets USP 12.5 mg contained Spironolactone Tablets USP 25 mg instead.
How can I tell if I have the recalled product?
Check for the label 'Hydrochlorothiazide Tablets USP 12.5 mg' on the bottle and verify the contents match the label. The product has NDC 16729-182-01 and lot number PW05264.
What should I do if I have the recalled product?
The recall record does not specify a remedy, so contact your pharmacy or healthcare provider for guidance.
Contact Accord Healthcare
We’ve drafted a message you can send Accord Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-1206-2018 — Accord Healthcare Accord Healthcare Hello, I own a Accord Healthcare that is covered by recall D-1206-2018 from Accord Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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-1206-2018 (August 21, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1206-2018 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.