S-Series Equipment Management System recall in Canada: patient injury risk
In plain language
This recall involves the S-Series Equipment Management System sold in Canada. It's being recalled because a part may disengage when an electrocautery device is used, which could cause patient injury. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check model and serial numbers.
- Contact Stryker Communications Inc. for more information.
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
S-Series Equipment Management Syetem
Model: 0682-400-550
Lot: 2258046-2863490
Why this matters
Patient injury risk
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: 2258046-2863490
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 0682-400-550
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?
Patient injury risk
What should consumers do?
Stop using the product immediately. Check model and serial numbers. Contact Stryker Communications Inc. for more 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. Patient injury risk
When was this product recalled?
This product was recalled on February 19, 2021.