Randox G-6-PDH Control Recalled: Incorrect Target Values for Diagnostics

Take action

Contact the company & request your remedy

Recalling firmRandox Laboratories Ltd.55 Diamond Road, N/A · Crumlin (North), N/A N/A

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Randox is recalling a blood test control product (G-6-PDH Deficient Control) because the target values in certain lots are incorrect. This could lead to inaccurate blood test results if used improperly.

Why it’s dangerous

The product is designed to check glucose-6-phosphate dehydrogenase levels in blood cells. Incorrect target values in specific lots could cause inaccurate test results, potentially affecting diagnosis.

Who’s affected

Lab technicians and healthcare providers who use this blood test control product for quality checks. Those using the recalled lots (687PD, 700PD, 715PD) are most at risk.

How to tell if you have this one

Check the lot number on the product label. The recalled lots are 687PD, 700PD, and 715PD. This product is used for in vitro diagnostic testing.

Brand
Randox
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Lot Number
Look for the lot number on the product label. The recalled lots are 687PD, 700PD, and 715PD.

✎ GovInfoNow

Questions people ask

What is the product name?

G-6-PDH Deficient Control (G-6-PDH CONTROL D), Catalogue Number PD2617.

Which lots are affected?

Lots 687PD, 700PD, and 715PD.

Why is this product being recalled?

The target values and ranges in these lots are incorrect, which could lead to inaccurate blood test results.

Take action

Contact Randox

We’ve drafted a message you can send Randox to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1254-2019 — Randox Randox

Hello,

I own a Randox that is covered by recall Z-1254-2019 from Randox.

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

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 #Z-1254-2019 (April 3, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1254-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 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.

Randox Laboratories Ltd. recalls G-6-PDH Deficient Control (G-6-PDH CONTROL D), Catalogue Number PD2617 Product Usage: This product is intended for in

Lower-risk recall