Public recall detail

AirSeal Access Port With Blunt Obturator and AirSeal Access Port With Optical Obturator

2026-07-02

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Health products Health product recall
Quick summary

Quick summary: AirSeal Access Port With Blunt Obturator and AirSeal Access Port With Optical Obturator. Reason: Health product recall. Category: Health products. Date: 2026-07-02.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: AirSeal Access Port With Blunt Obturator and AirSeal Access Port With Optical Obturator. Reason: Health product recall. Category: Health products. Date: 2026-07-02.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandConmed Corporation
ProductAirSeal Access Port With Blunt Obturator and AirSeal Access Port With Optical Obturator
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82267

Affected products

ProductAirSeal Access Port With Blunt Obturator
LotMore than 10 numbers, contact manufacturer.
ModelIASB12-100
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAirSeal Access Port With Blunt Obturator
ProductAirSeal Access Port With Blunt Obturator
LotMore than 10 numbers, contact manufacturer.
ModelIASB5-150
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAirSeal Access Port With Blunt Obturator
ProductAirSeal Access Port With Blunt Obturator
LotMore than 10 numbers, contact manufacturer.
ModelIASB12-120
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAirSeal Access Port With Blunt Obturator
ProductAirSeal Access Port With Optical Obturator
LotMore than 10 numbers, contact manufacturer.
ModelIAS12-150LPI
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAirSeal Access Port With Optical Obturator
ProductAirSeal Access Port With Optical Obturator
LotMore than 10 numbers, contact manufacturer.
ModelIAS12-100LPI
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAirSeal Access Port With Optical Obturator
ProductAirSeal Access Port With Optical Obturator
LotMore than 10 numbers, contact manufacturer.
ModelIAS5-75LP
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAirSeal Access Port With Optical Obturator
ProductAirSeal Access Port With Optical Obturator
LotMore than 10 numbers, contact manufacturer.
ModelIAS8-100LP
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAirSeal Access Port With Optical Obturator
ProductAirSeal Access Port With Optical Obturator
LotMore than 10 numbers, contact manufacturer.
ModelIAS8-120LP
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAirSeal Access Port With Optical Obturator
ProductAirSeal Access Port With Optical Obturator
LotMore than 10 numbers, contact manufacturer.
ModelIAS5-100LP
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAirSeal Access Port With Optical Obturator
ProductAirSeal Access Port With Optical Obturator
LotMore than 10 numbers, contact manufacturer.
ModelIAS12-120LPI
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAirSeal Access Port With Optical Obturator
ProductAirSeal Access Port With Optical Obturator
LotMore than 10 numbers, contact manufacturer.
ModelIAS5-120LP
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAirSeal Access Port With Optical Obturator

Issue

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 you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - General and plastic surgery
CompaniesConmed Corporation525 French Rd., Utica, New York, United States, 13502-5994
Recall date2026-06-04
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82267
Background{}
CompaniesConmed Corporation525 French Rd., Utica, New York, United States, 13502-5994
AudiencesHealthcare
Source updated2026-07-02

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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