OFFICIAL-SOURCE RECALL · CANADA
Radiography 7000 M Recall: Philips has become aware of a potential safety issue
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- See official notice
- Product
- Radiography 7000 M
- Manufacturer
- See official notice
- Model number
- 712010
The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.
Why this product was recalled
Philips has become aware of a potential safety issue impacting the Radiography 7000 M system (Model 712010) where the drive function may fail immediately after an exposure, causing the system to remain stationary. The issue may occur with the Radiography 7000 M system immediately after an exposure, causing the drive function to fail and preventing repositioning of the system. The system may remain stationary instead of driving upon activation of the handlebar. The issue is intermittent and has been observed during routine mobile radiography use.
Hazard
Philips has become aware of a potential safety issue impacting the Radiography 7000 M system (Model 712010) where the drive function may fail immediately after an exposure, causing the system to remain stationary. The issue may occur with the Radiography 7000 M system immediately after an exposure, causing the drive function to fail and preventing repositioning of the system. The system may remain stationary instead of driving upon activation of the handlebar. The issue is intermittent and has been observed during routine mobile radiography use.
Official recall notice
Radiography 7000 M
Agency: Health Canada
Official publication date: October 1, 2026
Read the official CANADA_MEDICAL_DEVICES recall notice →SCAN ONCE. KEEP WATCHING.
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