Health product recall

LIFEPAK ® 35 Monitor/Defibrillator

Last updated

Summary

Product
LIFEPAK ® 35 Monitor/Defibrillator
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information.

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalogue number

LIFEPAK ® 35 Monitor/Defibrillator

More than 10 numbers, contact manufacturer.

70335-000180

LIFEPAK ® 35 Monitor/Defibrillator

More than 10 numbers, contact manufacturer.

99335-000123

LIFEPAK ® 35 Monitor/Defibrillator

More than 10 numbers, contact manufacturer.

99335-000124

LIFEPAK ® 35 Monitor/Defibrillator

More than 10 numbers, contact manufacturer.

70335-000182

LIFEPAK ® 35 Monitor/Defibrillator

More than 10 numbers, contact manufacturer.

70335-000185

LIFEPAK ® 35 Monitor/Defibrillator

More than 10 numbers, contact manufacturer.

70335-000184

LIFEPAK ® 35 Monitor/Defibrillator

More than 10 numbers, contact manufacturer.

99335-000121

LIFEPAK ® 35 Monitor/Defibrillator

More than 10 numbers, contact manufacturer.

99335-000126

LIFEPAK ® 35 Monitor/Defibrillator

More than 10 numbers, contact manufacturer.

70335-000183

LIFEPAK ® 35 Monitor/Defibrillator

More than 10 numbers, contact manufacturer.

99335-000035

LIFEPAK ® 35 Monitor/Defibrillator

More than 10 numbers, contact manufacturer.

99335-000125

LIFEPAK ® 35 Monitor/Defibrillator

More than 10 numbers, contact manufacturer.

70335-000047

LIFEPAK ® 35 Monitor/Defibrillator

More than 10 numbers, contact manufacturer.

70335-000181

LIFEPAK ® 35 Monitor/Defibrillator

More than 10 numbers, contact manufacturer.

99335-000122

Issue

During production of LP35, Stryker identified that certain printer and modem access port connectors may not have been fully seated within the rear housing assembly. As a result, the connectors may appear flush with or recessed relative to the retaining nut rather than extending beyond it as intended. 

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies

Physio-Control, Inc.

11811 Willows Road North East, Redmond, Washington, United States, 98052

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-82601

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