Philips Achieva, Intera and Ingenia Systems recall in Canada: Laceration hazard
In plain language
This recall involves Philips Achieva, Intera, and Ingenia MRI systems used in healthcare settings in Canada. They are being recalled because a part of the system may create sharp edges that could cause injury to patients. Healthcare facilities should stop using the affected systems and follow the return/repair steps in the official notice.
What to do
- Stop using the affected systems immediately.
- Contact the manufacturer for additional information.
- Ensure the systems are kept away from patients until repaired or replaced.
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Affected products
Achieva XR System-Main Unit
Model: ACHIEVA XR
Achieva 3.0T MRI System-Main Unit
Model: ACHIEVA 3.0T
Intera 1.5T MRI System-Main Unit
Model: INTERA 1.5T
Achieva 1.5T MRI System-Main Unit
Model: ACHIEVA 1.5T
Ingenia 3.0T
Model: 3.0T
Why this matters
Laceration hazard from sharp edges
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: 3.0T, ACHIEVA 1.5T, ACHIEVA 3.0T, ACHIEVA XR, INTERA 1.5T
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?
Laceration hazard from sharp edges
What should consumers do?
Stop using the affected systems immediately. Contact the manufacturer for additional information. Ensure the systems are kept away from patients until repaired or replaced.
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. Laceration hazard from sharp edges
When was this product recalled?
This product was recalled on January 17, 2024.
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 Philips Achieva, Intera, and Ingenia MRI systems used in healthcare settings in Canada. They are being recalled because a part of the system may create sharp edges that could cause injury to patients. Healthcare facilities should stop using the affected systems and follow the return/repair steps in the official notice.