HIGHFDA DEVICE

DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.

System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.

Philips North AmericaHealth & Personal CareMedical DevicesModel Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
May 1, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
May 1, 2026
Hazard Level
HIGH
Brand
Philips North America

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Philips North America
Model numbers
Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    May 1, 2026

  2. Reported by FDA DEVICE

    June 17, 2026

  3. RecallRadar source check

    June 23, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Philips North America Llc or your healthcare provider for instructions. Notification method: Letter

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Full Description

DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.. Reason: System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.. Classification: Class II. Quantity: 1 unit. Distribution: US distribution to California.

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.
Report Date
June 17, 2026
Recall Status
ACTIVE

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