Public recall detail

Fluoroplastic Vent Tube

2026-10-06

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Health products Health product recall
Quick summary

Quick summary: Fluoroplastic Vent Tube. Reason: Health product recall. Category: Health products. Date: 2026-10-06.

Recommended action

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

Recall details

Quick summary: Fluoroplastic Vent Tube. Reason: Health product recall. Category: Health products. Date: 2026-10-06.

Official details

Affected product details

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

BrandMedtronic Xomed Inc.
ProductFluoroplastic Vent Tube
IssueMedical devices - Sterility
Recall classType II
IdentificationRA-82740

Affected products

ProductFluoroplastic Vent Tube
Lot0231048280
Model1013301
Serial number0231048280
DescriptionFluoroplastic Vent Tube

Issue

Vent tube devices across lot 0231048280 were identified to have been released to customers without undergoing sterilization. the issue is currently understood to originate from manufacturing (load preparation) and represents a fault condition: the product does not meet its specification for sterility (SAL 10-6) or its labeled sterile state.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Ear, nose and throat
CompaniesMedtronic Xomed Inc. 6743 Southpoint Drive North, Jacksonville, Florida, United States, 32216
Recall date2026-09-24
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82740
Background{}
CompaniesMedtronic Xomed Inc. 6743 Southpoint Drive North, Jacksonville, Florida, United States, 32216
AudiencesHealthcare
Source updated2026-10-06

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

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