Official recall record
AirSeal Access Port With Blunt Obturator and AirSeal Access Port With Optical Obturator
- Issuing authority
- Health Canada
- Alert date
- 2026-07-02
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
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. Image was added to IFU to reinforce proper device tightening. No injuries or deaths have been reported.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — official record →
Record last checked against the registry on 2026-07-12.
Record last checked against the registry on 2026-07-12.
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