Accord Healthcare, Inc. recalls Hydrochlorothiazide Tablets USP, 12.5 mg, 100-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Durham,
Product Mix-Up: customer complaint that a sealed bottle labeled as Hydrochlorothiazide Tablets USP 12.5 mg contained only Spironolactone Tablets USP 25 mg.
Recall notice
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
We’re still writing up this recall
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
Source Page by GovInfoNow · govinfonow.com/recall/39696-accord-healthcare-inc-recalls-hydrochlorothiazide-tablets-usp-12-5-mg · Recall date August 21, 2018 · FDA enforcement record: FDA #D-1206-2018
Cite this page
“Accord Healthcare, Inc. recalls Hydrochlorothiazide Tablets USP, 12.5 mg, 100-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Durham,.” GovInfoNow, recall dated August 21, 2018. https://govinfonow.com/recall/39696-accord-healthcare-inc-recalls-hydrochlorothiazide-tablets-usp-12-5-mg. Based on FDA recall #D-1206-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1206-2018%22&limit=1).
How to tell if you have this one
- Brand
ACCORD HEALTHCARE, INC.- Category
Drug
Contact ACCORD HEALTHCARE, INC.
We’ve drafted a message you can send ACCORD HEALTHCARE, INC. to request your refund or repair — edit it as you like.
Subject: Recall D-1206-2018 — ACCORD HEALTHCARE, INC. Accord Healthcare, Inc. recalls Hydrochlorothiazide Tablets USP, 12.5 mg, 1 Hello, I own a Accord Healthcare, Inc. recalls Hydrochlorothiazide Tablets USP, 12.5 mg, 100-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Durham, that is covered by recall D-1206-2018 from ACCORD HEALTHCARE, INC.. 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.
Similar recalls
Keep exploring
From people who’ve dealt with this
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
- 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.