Brightview System recall in Canada: extremity entrapment hazard
In plain language
This recall involves Brightview Gamma Camera Systems sold in Canada. They are being recalled because they may pose an extremity entrapment hazard to patients during a scan. Healthcare providers should contact the manufacturer for more information.
What to do
- Stop using the product immediately.
- Check model numbers.
- Contact the manufacturer for additional information.
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
Brightview Gamma Camera Sy. W/ 3/4" Crystal & Detector Caudal And Cephalic Tilt
Model: 2170-3003A
Brightview Gamma Camera Sy. W/ 3/8" Crystal & Detector Caudal Cephalic Tilt
Model: 2170-3002A
Brightview Gamma Camera System With 3/8" Crystal
Model: 2170-3000A
Brightview Gamma Camera System With 3/4" Crystal
Model: 2170-3001A
Why this matters
Extremity entrapment hazard
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 2170-3000A, 2170-3001A, 2170-3002A, 2170-3003A
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Extremity entrapment hazard
What should consumers do?
Stop using the product immediately. Check model numbers. Contact the manufacturer for additional information.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Extremity entrapment hazard
When was this product recalled?
This product was recalled on December 22, 2023.
Is the PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. brand affected by this recall?
Yes, PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. products are affected by this recall. This recall involves Brightview Gamma Camera Systems sold in Canada. They are being recalled because they may pose an extremity entrapment hazard to patients during a scan. Healthcare providers should contact the manufacturer for more information.