Pentacam Axl recall in Canada: Performance issue
In plain language
This recall involves the Pentacam Axl, a medical device used in ophthalmology. It's being recalled because the IOL calculator printout may not accurately reflect alignment and incision position for toric IOLs. Healthcare professionals should contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Pentacam Axl
Lot: 70100 0931 7150, 70100 5261 7121, 70100 3032 1270, 70100 0831 7150, 70100 9891 9170, 70100 7881 9120
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 lot number
Lot numbers identify specific production batches.
Affected lots: 70100 0931 7150, 70100 5261 7121, 70100 3032 1270, 70100 0831 7150, 70100 9891 9170, 70100 7881 9120
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?
This recall involves the Pentacam Axl, a medical device used in ophthalmology. It's being recalled because the IOL calculator printout may not accurately reflect alignment and incision position for toric IOLs. Healthcare professionals should contact the manufacturer for more information.
What should consumers do?
Contact the manufacturer if you require 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?
A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.
When was this product recalled?
This product was recalled on July 25, 2022.
Is the Oculus Optikgeraete Gmbh brand affected by this recall?
Yes, Oculus Optikgeraete Gmbh products are affected by this recall. This recall involves the Pentacam Axl, a medical device used in ophthalmology. It's being recalled because the IOL calculator printout may not accurately reflect alignment and incision position for toric IOLs. Healthcare professionals should contact the manufacturer for more information.