Ambu SPUR II Resuscitator recall in Canada: Performance issue
In plain language
This recall involves Ambu SPUR II Adult and Pediatric Resuscitators sold in Canada. They are being recalled because a blocked manometer port can prevent pressure monitoring. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Discard the affected products.
- Contact the manufacturer for a refund or replacement.
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Affected products
Ambu® SPUR®II Adult Resuscitator
Model: 523211000, 524611000
Lot: 1001110297, 1001113554, 1001118764
Ambu® SPUR®II Pediatric Resuscitator
Model: 530213000, 530213001, 530213031, 530214000, 530613000, 530613031
Lot: 1001106634, 1001106635, 1001106636, 1001106637, 1001110299, 1001113558, 1001113560, 1001118767, 2000015889
Why this matters
Risk of barotrauma or procedural delays
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: 1001106634, 1001106635, 1001106636, 1001106637, 1001110297, 1001110299, 1001113554, 1001113558, 1001113560, 1001118764, 1001118767, 2000015889
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 523211000, 524611000, 530213000, 530213001, 530213031, 530214000, 530613000, 530613031
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?
Risk of barotrauma or procedural delays
What should consumers do?
Stop using the product immediately. Discard the affected products. Contact the manufacturer for a refund or replacement.
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. Risk of barotrauma or procedural delays
When was this product recalled?
This product was recalled on July 23, 2025.
Is the Ambu A/S brand affected by this recall?
Yes, Ambu A/S products are affected by this recall. This recall involves Ambu SPUR II Adult and Pediatric Resuscitators sold in Canada. They are being recalled because a blocked manometer port can prevent pressure monitoring. Stop using the product and follow the return steps in the official notice.