HIGHFDA DEVICE

Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.

Software anomaly that causes a false display of error code 5018.

IPG MedicalHealth & Personal CareMedical DevicesModel No. MD2300F-001507UDI-DI 00810071230226Serial No. MDUF250342

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
May 5, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
May 5, 2026
Hazard Level
HIGH
Brand
IPG Medical
Geographic Scope
1 states

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
IPG Medical
Model numbers
Model No. MD2300F-001507, UDI-DI 00810071230226, Serial No. MDUF250342, MDUF250400, MDUF250429, MDUF250060, MDUF250061, MDUF250067 +12 more
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    May 5, 2026

  2. Reported by FDA DEVICE

    July 1, 2026

  3. RecallRadar source check

    July 7, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

Software anomaly that causes a false display of error code 5018.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact IPG Medical Corporation or your healthcare provider for instructions. Notification method: E-Mail

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Full Description

Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.. Reason: Software anomaly that causes a false display of error code 5018.. Classification: Class II. Quantity: 198 units. Distribution: US Nationwide distribution in the state of MA.

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 No. MD2300F-001507
UDI-DI 00810071230226
Serial No. MDUF250342
MDUF250400
MDUF250429
+15 more
Affected States
ALL
Report Date
July 1, 2026
Recall Status
ACTIVE