Public recall detail

LIFEPAK 15 V4 SpCO/SpMet Sensors

2026-05-21

medium
Health products Health product recall
Quick summary

Quick summary: LIFEPAK 15 V4 SpCO/SpMet Sensors. Reason: Health product recall. Category: Health products. Date: 2026-05-21.

Recommended action

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

Recall details

Quick summary: LIFEPAK 15 V4 SpCO/SpMet Sensors. Reason: Health product recall. Category: Health products. Date: 2026-05-21.

Official details

Affected product details

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

BrandPhysio-Control, Inc.
ProductLIFEPAK 15 V4 SpCO/SpMet Sensors
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82104

Affected products

ProductLNCS-II Rainbow DCIP 8 SpCO
Lot23JBP
Model4068
Serial number23JBP
DescriptionLNCS-II Rainbow DCIP 8 SpCO
ProductLNCS-II Rainbow DCI 8 SpCO
Lot23HPT
Model4067
Serial number23HPT
DescriptionLNCS-II Rainbow DCI 8 SpCO
ProductLNCS-II Rainbow DCI 8 SpCO
Lot23HER
Model4067
Serial number23HER
DescriptionLNCS-II Rainbow DCI 8 SpCO
ProductLNCS-II Rainbow DCI 8 SpCO
Lot23JTA
Model4067
Serial number23JTA
DescriptionLNCS-II Rainbow DCI 8 SpCO
ProductLNCS-II Rainbow DCI 8 SpCO
Lot23GJQ
Model4067
Serial number23GJQ
DescriptionLNCS-II Rainbow DCI 8 SpCO
ProductLNCS-II Rainbow DCI 8 SpCO
Lot23JBN
Model4067
Serial number23JBN
DescriptionLNCS-II Rainbow DCI 8 SpCO
ProductRD Rainbow SpCO
Lot23JAU
Model4036
Serial number23JAU
DescriptionRD Rainbow SpCO

Issue

Stryker received complaints indicating that the LIFEPAK 15 V4 displayed an error where “SpO2: Sensor does not support SpCO or SpMET.” The error results in preventing users from utilizing LIFEPAK 15 V4 SpCO and SpMet functionalities when connected to specific lots of Masimo Rainbow Sensors. The specific sensor lots are compatible with the LIFEPAK 15 V1 and V2 devices.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Anaesthesiology
CompaniesPhysio-Control, Inc. 11811 Willows Road North East, Redmond, Washington, United States, 98052
Recall date2026-05-11
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82104
Background{}
CompaniesPhysio-Control, Inc. 11811 Willows Road North East, Redmond, Washington, United States, 98052
AudiencesHealthcare
Source updated2026-05-21

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

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