Public recall detail

LIFEPAK ® 35 Monitor/Defibrillator

2026-09-02

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Health products Health product recall
Quick summary

Quick summary: LIFEPAK ® 35 Monitor/Defibrillator. Reason: Health product recall. Category: Health products. Date: 2026-09-02.

Recommended action

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

Recall details

Quick summary: LIFEPAK ® 35 Monitor/Defibrillator. Reason: Health product recall. Category: Health products. Date: 2026-09-02.

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 ® 35 Monitor/Defibrillator
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82590

Affected products

ProductLIFEPAK ® 35 Monitor/Defibrillator
LotMore than 10 numbers, contact manufacturer.
Model70335-000180
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionLIFEPAK ® 35 Monitor/Defibrillator
ProductLIFEPAK ® 35 Monitor/Defibrillator
LotMore than 10 numbers, contact manufacturer.
Model99335-000123
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionLIFEPAK ® 35 Monitor/Defibrillator
ProductLIFEPAK ® 35 Monitor/Defibrillator
LotMore than 10 numbers, contact manufacturer.
Model99335-000124
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionLIFEPAK ® 35 Monitor/Defibrillator
ProductLIFEPAK ® 35 Monitor/Defibrillator
LotMore than 10 numbers, contact manufacturer.
Model70335-000182
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionLIFEPAK ® 35 Monitor/Defibrillator
ProductLIFEPAK ® 35 Monitor/Defibrillator
LotMore than 10 numbers, contact manufacturer.
Model70335-000185
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionLIFEPAK ® 35 Monitor/Defibrillator
ProductLIFEPAK ® 35 Monitor/Defibrillator
LotMore than 10 numbers, contact manufacturer.
Model99335-000126
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionLIFEPAK ® 35 Monitor/Defibrillator
ProductLIFEPAK ® 35 Monitor/Defibrillator
LotMore than 10 numbers, contact manufacturer.
Model70335-000184
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionLIFEPAK ® 35 Monitor/Defibrillator
ProductLIFEPAK ® 35 Monitor/Defibrillator
LotMore than 10 numbers, contact manufacturer.
Model99335-000121
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionLIFEPAK ® 35 Monitor/Defibrillator
ProductLIFEPAK ® 35 Monitor/Defibrillator
LotMore than 10 numbers, contact manufacturer.
Model70335-000183
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionLIFEPAK ® 35 Monitor/Defibrillator
ProductLIFEPAK ® 35 Monitor/Defibrillator
LotMore than 10 numbers, contact manufacturer.
Model99335-000035
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionLIFEPAK ® 35 Monitor/Defibrillator
ProductLIFEPAK ® 35 Monitor/Defibrillator
LotMore than 10 numbers, contact manufacturer.
Model99335-000125
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionLIFEPAK ® 35 Monitor/Defibrillator
ProductLIFEPAK ® 35 Monitor/Defibrillator
LotMore than 10 numbers, contact manufacturer.
Model70335-000047
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionLIFEPAK ® 35 Monitor/Defibrillator
ProductLIFEPAK ® 35 Monitor/Defibrillator
LotMore than 10 numbers, contact manufacturer.
Model70335-000181
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionLIFEPAK ® 35 Monitor/Defibrillator
ProductLIFEPAK ® 35 Monitor/Defibrillator
LotMore than 10 numbers, contact manufacturer.
Model99335-000122
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionLIFEPAK ® 35 Monitor/Defibrillator

Issue

Stryker has identified an issue with the LP35 where the device does not display the message "CHECK RHYTHM / ECG Analysis Inconclusive" as intended when specific conditions are present simultaneously. The issue does not affect the display of "shock advised" or "no shock advised" messages, and therapy delivery remains available. Additionally, this nonconformance is limited to the device on-screen prompts only; rhythm analysis is not impacted by this issue.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Cardiovascular
CompaniesPhysio-Control, Inc. 11811 Willows Road North East, Redmond, Washington, United States, 98052
Recall date2026-08-27
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82590
Background{}
CompaniesPhysio-Control, Inc. 11811 Willows Road North East, Redmond, Washington, United States, 98052
AudiencesHealthcare
Source updated2026-09-02

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

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