Philips Azurion FlexArm 722: Power Cable Damage Risk

Take action

Contact the company & request your remedy

Recalling firmPhilips North America, LLC3000 Minuteman Rd, N/A · Andover, MA 01810-1032

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

Philips is recalling specific Azurion FlexArm models with serial numbers 637 and 638 because manufacturing defects could damage the 24V power cable. This may lead to equipment malfunction or safety issues if not addressed.

Why it’s dangerous

During manufacturing, the 24V power cable in the Azurion R2.0 system was not made to specification. This defect could cause the cable to damage, potentially leading to equipment malfunction or safety issues.

Who’s affected

Users of Philips Azurion FlexArm models 722079 with serial numbers 637 and 638 are affected. Medical professionals using these devices for imaging are most at risk due to potential equipment failure.

How to tell if you have this one

Check for Azurion FlexArm model 722079 with serial numbers 637 or 638. This recall applies to specific units sold in the U.S. market.

Brand
Philips
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Serial Number
Identify the serial number on your Azurion FlexArm device to confirm if it is 637 or 638.

✎ GovInfoNow

Questions people ask

What is the specific model number for this recall?

The recalled model is Azurion FlexArm 722079 with serial numbers 637 and 638.

Why is this recall happening?

During manufacturing, the 24V power cable was not made to specification, potentially causing damage.

Do I need to stop using this device immediately?

No immediate stop is required; the recall involves specific units that may need repair or replacement.

Take action

Contact Philips

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

✉️ Open in email

Subject: Recall Z-1130-2019 — Philips Philips

Hello,

I own a Philips that is covered by recall Z-1130-2019 from Philips.

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-1130-2019 (March 12, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1130-2019 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.

Philips North America, LLC recalls Azurion FlexArm, 722079

Lower-risk recall