Recall StatusOpen, Classified
Date Initiated2023-03-09
Product QuantityUS: 10 units; OUS: 570 units
Reason for Recall
If the PM for the telescopic carriage is not performed annually as defined in the Instructions for Use (IFU), the tension force of the spring balancer inside of the telescopic carriage will unavoidably decay through
normal wear and tear; as a result there is a potential that the Ceiling Suspension of the DigitalDiagnost C50 system may descend inadvertently if power to the system is interrupted, and may result in injuries to patients and users
Firm Action
Philips issued Urgent Medical Device Correction Letter to US Consignees on 09-Mar-2023.
Letter states reason for recall, health risk and action to take:
Follow the Planned Maintenance Program in the Addendum to the Instructions for Use in
Appendix A of this notice for the safe use of your system(s).
" If the Ceiling Suspension is not able to be kept in its current position by itself and descends
after the power to the system is off, contact your local Philips representative to perform the
maintenance of the telescopic carriage.
" Place this URGENT Medical Device Correction Notice with the documentation of your system(s).
" Complete the enclosed Customer Reply Form and send it back to confirm that users have reviewed and understood this URGENT Medical Device Correction Notice.
Philips is informing customers through this URGENT Medical Device Correction Notice and providing
the Addendum to the Instructions for Use of the DigitalDiagnost C50 system.
If you need additional information or support concerning this issue, please contact the Customer Care -9377).
Root Cause
Equipment maintenance
Distribution Pattern
Nationwide including Puerto Rico and Virgin Islands
Foreign:
ARGENTINA
Australia
Austria
Bosnia and Herzegovina
Bulgaria
China
Colombia
Cyprus
Czech Republic
Egypt
France
French Polynesia
Germany
Greece
Hungary
Indonesia
Italy
Jordan
Kenya
Latvia
Lithuania
Macedonia
Malta
Mexico
Netherlands
New Zealand
Philippines
Poland
Portugal
Puerto Rico
Russian Federation
Saudi Arabia
Serbia
Slovenia
South Africa
Spain
Sri Lanka
Switzerland
Tanzania
Thailand
United Arab Emirates
Viet Nam
Yemen
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.