SEDECAL AeroDR X30 X-Ray Systems Not Water-Resistant; Clean Care Required

Take action

Contact the company & request your remedy

Recalling firmSEDECAL SAPelaya, 9 Pol., Pol. Ind. Rio De Janeiro · Algete, N/A

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

SEDECAL is recalling its AeroDR X30 mobile X-ray systems because they are not water-resistant. If cleaned improperly, the equipment could be damaged. This affects medical facilities using these devices.

Why it’s dangerous

The devices are not designed to be water-resistant. If cleaned improperly, they could become damaged. This damage might affect the equipment's functionality and safety.

Who’s affected

Medical facilities that own or use the recalled AeroDR X30 mobile X-ray systems. Staff handling the equipment during cleaning are most at risk of damage.

How to tell if you have this one

Check for the model name 'AeroDR X30' and serial numbers listed in the recall notice. The equipment was sold with the UDI/DI 084360460: 20+ specific serial numbers.

Brand
SEDECAL
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Cleaning Instructions
Review the device's manual for proper cleaning procedures to avoid damage.

✎ GovInfoNow

Questions people ask

Why is this recall happening?

The equipment is not water-resistant and must be cleaned strictly according to the manual to prevent damage.

What happens if I clean it improperly?

Improper cleaning could damage the equipment, potentially affecting its functionality and safety.

How can I tell if my device is recalled?

Look for the model name 'AeroDR X30' and check if your serial number is listed in the provided list of 20+ numbers.

Take action

Contact SEDECAL

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

✉️ Open in email

Subject: Recall Z-0242-2026 — SEDECAL SEDECAL

Hello,

I own a SEDECAL that is covered by recall Z-0242-2026 from SEDECAL.

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-0242-2026 (June 10, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0242-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.

SEDECAL SA recalls Sedecal Mobile Digital Diagnostic X-Ray Systems; SM-40HF-B-D-KM (AeroDR X30)

Lower-risk recall