Health product recall

Azurion and Allura Systems

Last updated

Summary

Product
Azurion and Allura Systems
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products Lot or serial number Model or catalog number
Allura Xper FD10 Not applicable. 001443
Allura Xper FD20 OR Table (Product Of AlluraClarity Family) Not applicable. 722035
Allura Xper FD20/10 (Product Of AlluraClarity Family) Not applicable. 722029
Allura Xper FD20/15 Not applicable. 722058
Azurion 7 M20 Not applicable. 722 224 722 079 722234
Azurion 3 M12 Not applicable. 722 063 722 221
Azurion 3 M15 Not applicable. 722 064 722 222
Azurion 7 B12 Not applicable. 722 067 722235 722 225
Allura Xper FD10/10 (Product Of AlluraClarity Family) Not applicable. 722027
Azurion 7 M12 Not applicable. 722233 722 223 722 078
Allura Xper FD10 (Product Of AlluraClarity Family) Not applicable. 722026
Allura Xper FD20 (Product Of AlluraClarity Family) Not applicable. 722028
Allura Xper FD20/20 (Product Of AlluraClarity Family) Not applicable. 722038
Azurion 7 B20 Not applicable. 722 226 722236 722 068
Azurion 5 M12 Not applicable. 722 227 722231
Azurion 5 M20 Not applicable. 722 228 722232

Issue

Philips has identified that during manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop, possibly resulting in an injury of the finger. The risk is applicable for the operators and service personnel.

Recall start date: January 17, 2025

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Radiology
Companies

Philips Medical Systems Nederland B.V.

Veenpluis 6, Best, Netherlands, 5684 PC

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-76885

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