HL7 Outbound Results Interface recall in Canada: Software defect
In plain language
This recall involves the HL7 Outbound Results Interface from Omnitech Labs Inc. sold in Canada. It's being recalled because a software defect could cause patient results to be assigned incorrectly. Stop using the product and contact the manufacturer for more information.
What to do
- Stop using the product immediately.
- Check model numbers: HL7-REO v18.4.0.17 V12.
- Contact Omnitech Labs Inc. for additional information.
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Affected products
HL7 Outbound Results Interface
Model: HL7-REO v18.4.0.17 V12
Why this matters
Incorrect patient data assignment
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: HL7-REO v18.4.0.17 V12
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?
Incorrect patient data assignment
What should consumers do?
Stop using the product immediately. Check model numbers: HL7-REO v18.4.0.17 V12. Contact Omnitech Labs Inc. 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. Incorrect patient data assignment
When was this product recalled?
This product was recalled on August 4, 2022.
Is the Omnitech Labs Inc. brand affected by this recall?
Yes, Omnitech Labs Inc. products are affected by this recall. This recall involves the HL7 Outbound Results Interface from Omnitech Labs Inc. sold in Canada. It's being recalled because a software defect could cause patient results to be assigned incorrectly. Stop using the product and contact the manufacturer for more information.