No image published for this recall

Airseal access port with blunt obturator and airseal access port with optical obturator

Official notice

2 Jul 2026

MediumHealth Canada

An official Health Canada notice concerns Airseal access port with blunt obturator and airseal access port with optical obturator. 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. Published 2026-07-02.

What to do now

Contact the manufacturer if you require additional information.

Recall number

82267

Official notice

2026-07-02

The hazard

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.

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Skus

IASB12-100, IASB5-150, IASB12-120, IAS12-150LPI, IAS12-100LPI, IAS5-75LP, IAS8-100LP, IAS8-120LP, IAS5-100LP, IAS12-120LPI, IAS5-120LP

Other

RA RA-82267

Model Numbers

IASB12-100, IASB5-150, IASB12-120, IAS12-150LPI, IAS12-100LPI, IAS5-75LP, IAS8-100LP, IAS8-120LP, IAS5-100LP, IAS12-120LPI, IAS5-120LP

Recall Numbers

82267

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Affected products

Product 1

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - IASB12-100

Product 2

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - IASB5-150

Product 3

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - IASB12-120

Product 4

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - IAS12-150LPI

Product 5

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - IAS12-100LPI

Product 6

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - IAS5-75LP

Product 7

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - IAS8-100LP

Product 8

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - IAS8-120LP

Product 9

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - IAS5-100LP

Product 10

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - IAS12-120LPI

Product 11

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - IAS5-120LP

Risk / hazard

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.

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Brand

Manufacturer

Not provided

Phone

Not provided

Brand: Conmed.

Source & status

Source

Health Canada

Tier

beta

Category

HOME

Classification

Type II

App estimate

medium

Recall details

Recall number

82267

Classification

Type II

Source tier

beta

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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