HIGHFDA DEVICE

Philips CT 6000 CT Scanner Recall 6-Unit for Table Descent Risk (2025)

Philips North America recalled 6 CT 6000 scanners, Model 728307, distributed worldwide including the United States. The patient support table may descend unexpectedly to the lowermost position due to ball screw misalignment after a replacement. Stop using the device immediately and follow manufacturer instructions. Contact Philips for guidance and next steps.

Official notice
PhilipsHealth & Personal CareMedical DevicesCT 6000, Model Number: 728307UDI-DI: 00884838104600Serial Numbers: 87150

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
August 13, 2025
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
August 13, 2025
Hazard Level
HIGH
Brand
Philips
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

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
Product type
CT Scanner
Model numbers
CT 6000, Model Number: 728307, UDI-DI: 00884838104600, Serial Numbers: 87150, 87169, 87118, 87168, 87166, 87164
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    August 13, 2025

  2. Reported by FDA DEVICE

    October 1, 2025

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.

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

About This Product

CT scanners are medical imaging devices used to diagnose a wide range of conditions. The Philips CT 6000 is a diagnostic imaging system used in hospital settings.

Why This Is Dangerous

A misaligned ball screw after replacement can cause the patient table to descend unexpectedly, potentially compromising patient safety during scanning.

Industry Context

This recall is not presented as part of a broader industry pattern in the provided information.

Real-World Impact

Hospitals and clinics must halt use of affected scanners until advised by Philips. The recall could affect diagnostic workflows and patient throughput.

Practical Guidance

How to identify if yours is affected

  1. Identify if you own a Philips CT 6000 with Model 728307 by checking the device label, user manual, and service records.
  2. Review the FDA recall notice for official instructions.

Where to find product info

Recall notices and service bulletins from Philips and the FDA enforcement page (recall number Z-2604-2025).

What timeline to expect

No remediation timeline is provided in the notice.

If the manufacturer is unresponsive

  • Escalate to hospital risk management or biomedical engineering.
  • Document all communications with Philips and the facility.
  • Consider filing a complaint with FDA if the company is unresponsive.

How to prevent similar issues

  • Ensure clear lines of communication with the vendor for post-replacement checks.

Documentation advice

Keep copies of the recall notice, service communications, serial numbers, and UDI-DI. Photograph labels and document any steps taken in response.

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

Product Details

Model: CT 6000, Model Number 728307. UDI-DI: 00884838104600. Serial Numbers: 87150, 87169, 87118, 87168, 87166, 87164. Quantity: 6 units. Distribution: Worldwide, including US nationwide and numerous countries listed by FDA. Sold date and price not specified. Manufacturer: Philips North America LLC.

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • Worldwide distribution including US
  • Status: ACTIVE; Hazard level: HIGH

Safety Guide

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

Read: What to Do When You Find a Recalled Product

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
CRUSHINGOTHER

Product Details

Brand
Model Numbers
CT 6000, Model Number: 728307
UDI-DI: 00884838104600
Serial Numbers: 87150
87169
87118
+3 more
Affected States
ALL
Report Date
October 1, 2025
Recall Status
ACTIVE

Related Recalls

Health & Personal Care
HIGH

Philips Tempus Pro Patient Monitor Recalled Over Accuracy Issues

Philips recalled 7,129 Tempus Pro Patient Monitors on November 26, 2025. The monitors may provide unvalidated measurements for Intracranial Pressure and Bladder Pressure. Incorrect readings could lead to critical clinical decisions.

Philips
Patient monitor
Read more