Public recall detail

ForeSight™ Oximeter Cable

2026-08-21

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Health products Health product recall
Quick summary

Quick summary: ForeSight™ Oximeter Cable. Reason: Health product recall. Category: Health products. Date: 2026-08-21.

Recommended action

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

Recall details

Quick summary: ForeSight™ Oximeter Cable. Reason: Health product recall. Category: Health products. Date: 2026-08-21.

Official details

Affected product details

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

BrandEdwards Lifesciences LLC
ProductForeSight™ Oximeter Cable
IssueMedical devices - Labelling and packaging
Recall classType II
IdentificationRA-82518

Affected products

ProductForeSight™ Oximeter Cable
LotNot applicable.
ModelHEMFSM10
Serial numberNot applicable.
DescriptionForeSight™ Oximeter Cable

Issue

This recall is regarding inaccurate StO2 readings from the HEMFSM10 ForeSight™ Oximeter Cable due to mispositioning of the sensor cables. Edwards has identified that during manufacturing, the laterality identification labels may be missing or inaccurately placed on the device. There is potential that the labels on the green cables may have been switched, with the channel 1 cable labeled as channel 2, and the channel 2 cable labeled as channel 1. This will lead to a mismatch as to the left and right values displayed on the monitor and what the labels indicate on the cables. Should this potential issue occur during use, the values displayed on the monitor will be switched and will represent the opposite region being monitored. Therefore, there is a potential for incorrect diagnosis, leading to potential delay of appropriate treatment. If either of the labels are missing, or the flag label and/or the sensor label do not match the channel label on the housing, contact the Technical Support. If the flag and sensor labels correctly correspond to the channel labels, there is no further action required.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Cardiovascular
CompaniesEdwards Lifesciences LLC 1 Edwards Way, Irvine, California, United States, 92614
Recall date2026-08-11
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82518
Background{}
CompaniesEdwards Lifesciences LLC 1 Edwards Way, Irvine, California, United States, 92614
AudiencesHealthcare
Source updated2026-08-21

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

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