Z-0462-2026 Class II Ongoing
FDA device recall Z-0462-2026 was initiated by Philips Medical Systems DMC GmbH on Oct 1, 2025 and is designated Class II. Reason for recall: Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion… The recall status is ongoing. Affected quantity: 17 units.
Recall details
- Product Type
- Devices
- Report Date
- Nov 19, 2025
- Initiation Date
- Oct 1, 2025
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 17 units
Product description
Reason for recall
Distribution pattern
Worldwide Distribution: US (Nationwide) Distribution and OUS (International) countries of: Australia, Austria, Bahrain, Belgium, Bosnia-Herz., Canada, Chile, Croatia, Denmark, Estonia, Finland, France, Germany, Ghana, Gibraltar, Guadeloupe, Indonesia, Iraq, Israel, Italy, Jordan, Kuwait, Kyrgyzstan, Latvia, Lithuania, Netherlands, New Zealand, Norway, Panama, Philippines, Poland, Portugal, R¿union, Samoa, Saudi Arabia, Singapore, South Africa, South Korea, Spain, Sweden, Switzerland, T¿rkiye, Turkmenistan, United Kingdom, Utd.Arab.Emir.,
Code information
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0462-2026
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026