AirSeal Access Port Recall Issued by Health Canada
Areazine synthesizes this Health Canada recall directly from Health Canada's official public data feed. See our methodology for full source attribution and refresh cadence.
Health Canada recalls multiple AirSeal Access Port models due to potential erroneous overpressure alerts that may cause loss of pneumoperitoneum and treatment delays.
What this Health Canada recall tells you, and what most readers miss
This notice was issued by Health Canada on August 1, 2026 and geographically references Canada. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - Product & Food Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, health-canada, medical-device.
What Happened
A complaint review identified a prior manufacturing process update that may cause erroneous overpressure alerts under certain conditions, potentially leading to loss of pneumoperitoneum and treatment delays. An image was added to the instructions for use to reinforce proper device tightening. No injuries or deaths have been reported.
Which Products Are Affected
The following products from Conmed Corporation are affected:
- AirSeal Access Port With Blunt Obturator (model IASB12-100)
- AirSeal Access Port With Blunt Obturator (model IASB5-150)
- AirSeal Access Port With Blunt Obturator (model IASB12-120)
- AirSeal Access Port With Optical Obturator (model IAS12-150LPI)
- AirSeal Access Port With Optical Obturator (model IAS12-100LPI)
- AirSeal Access Port With Optical Obturator (model IAS5-75LP)
- AirSeal Access Port With Optical Obturator (model IAS8-100LP)
Lot or serial numbers: More than 10 numbers per model; contact the manufacturer for details.
What You Should Do
Consumers should contact the manufacturer for information on affected lots and any required actions.
Why This Matters
The recall addresses a device issue that could lead to treatment delays during procedures requiring pneumoperitoneum.
Source
Original source: Health Canada Official Notice ↗
Related Product & Food Recalls
All Product & Food Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this Health Canada recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,402 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 1, 2026.
Frequently Asked Questions
Common questions about this Health Canada recall.