DeRoyal NEURO PACK Recall: Risk of Injury from Improper Use

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Recalling firmDeRoyal Industries Inc200 Debusk Ln, N/A · Powell, TN 37849-4703

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✎ GovInfoNow plain-language explainer

What happened, in plain English

DeRoyal is recalling NEURO PACK devices with specific lot numbers because they could cause injury if used improperly. This recall affects consumers who purchased these devices with the listed lot numbers.

Why it’s dangerous

The hazard description is incomplete in the recall record. No specific mechanism of injury or risk details are provided to explain why the product is dangerous.

Who’s affected

DeRoyal NEURO PACK device owners with Lot 57184744 (expiring 5/1/2026) or Lot 57685899 (expiring 3/1/2024) are affected. Anyone using these devices without proper guidance is at higher risk.

How to tell if you have this one

Check your DeRoyal NEURO PACK device for the lot number: Lot 57184744 (expires May 1, 2026) or Lot 57685899 (expires March 1, 2024).

Brand
DeRoyal
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Lot Number
Identify your DeRoyal NEURO PACK's lot number to see if it matches Lot 57184744 (expires May 1, 2026) or Lot 57685899 (expires March 1, 2024).

✎ GovInfoNow

Questions people ask

What lot numbers are affected by this recall?

Lot 57184744 (expires May 1, 2026) and Lot 57685899 (expires March 1, 2024).

How can I tell if my DeRoyal NEURO PACK is affected?

Check the lot number on your device; if it matches Lot 57184744 (expires May 1, 2026) or Lot 57685899 (expires March 1, 2024), it is affected.

What should I do if my device is affected?

The recall record does not specify a remedy, so contact DeRoyal Industries Inc for further instructions.

Take action

Contact DeRoyal

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

✉️ Open in email

Subject: Recall Z-0675-2023 — DeRoyal DeRoyal

Hello,

I own a DeRoyal that is covered by recall Z-0675-2023 from DeRoyal.

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 #Z-0675-2023 (November 3, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0675-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.

DeRoyal Industries Inc recalls DeRoyal NEURO PACK, REF 89-10171.06

Recall notice