DeRoyal Shoulder Arthroscopy Pack RF Recall: Steri Drapes Risk

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Contact the company & request your remedy

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

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

DeRoyal is recalling Shoulder Arthroscopy Packs that contain specific 3M Steri Drapes. These drapes may have been contaminated, posing a risk of infection during medical procedures.

Why it’s dangerous

The recalled Steri Drapes may contain contaminants that could lead to infections during surgical procedures. This risk is specific to medical settings where the drapes are used.

Who’s affected

Medical professionals using these packs for shoulder surgeries are most at risk. Patients receiving procedures with the recalled packs could also be affected.

How to tell if you have this one

Check for lot numbers 56391741 (expires 1/1/2023), 56617587 (expires 2/1/2025), or 57391604 (expires 1/1/2024) on the pack's label.

Brand
DeRoyal
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Lot Number
Look for lot numbers 56391741, 56617587, or 57391604 on the pack's label.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The recalled Steri Drapes may contain contaminants that could lead to infections during surgical procedures.

What should I do if I have this product?

Check the lot number on the pack. If it matches the recalled numbers, contact DeRoyal for further instructions.

Are there any safety risks for patients?

Patients undergoing surgery with the recalled packs could be at risk of infection if the drapes are contaminated.

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-0573-2023 — DeRoyal DeRoyal

Hello,

I own a DeRoyal that is covered by recall Z-0573-2023 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-0573-2023 (November 3, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0573-2023 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 SHOULDER ARTHORSCOPY PACK RF, REF 89-6628.09

Lower-risk recall