CanadaThe LIFEPAK 35 Monitor/Defibrillator is affected; listed catalogue numbers include 70335-000180, 99335-000123, 99335-000124, 70335-000182, 70335-000185, 70335-000184, 99335-000121, 99335-000126, 70335-000183, 99335-000035, 99335-000125, 70335-000047, 70335-000181 and 99335-000122, and more than 10 serial/lot numbers are affected—contact the manufacturer for specific serial/lot information. The recall was issued because certain printer and modem access port connectors may not have been fully seated in the rear housing and can appear flush with or recessed relative to the retaining nut rather than extending beyond it. Contact the manufacturer if you require additional information.
What's being recalled
Companies: Physio-Control, Inc., 11811 Willows Road North East, Redmond, Washington, United States, 98052.
How to identify it
Affected products: LIFEPAK ® 35 Monitor/Defibrillator; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: 70335-000180
Affected products: LIFEPAK ® 35 Monitor/Defibrillator; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: 99335-000123
Affected products: LIFEPAK ® 35 Monitor/Defibrillator; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: 99335-000124
Affected products: LIFEPAK ® 35 Monitor/Defibrillator; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: 70335-000182
Affected products: LIFEPAK ® 35 Monitor/Defibrillator; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: 70335-000185
Affected products: LIFEPAK ® 35 Monitor/Defibrillator; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: 70335-000184
Affected products: LIFEPAK ® 35 Monitor/Defibrillator; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: 99335-000121
Affected products: LIFEPAK ® 35 Monitor/Defibrillator; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: 99335-000126
Affected products: LIFEPAK ® 35 Monitor/Defibrillator; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: 70335-000183
Affected products: LIFEPAK ® 35 Monitor/Defibrillator; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: 99335-000035
Affected products: LIFEPAK ® 35 Monitor/Defibrillator; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: 99335-000125
Affected products: LIFEPAK ® 35 Monitor/Defibrillator; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: 70335-000047
Affected products: LIFEPAK ® 35 Monitor/Defibrillator; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: 70335-000181
Affected products: LIFEPAK ® 35 Monitor/Defibrillator; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: 99335-000122
The hazard
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.
What to do
Contact the manufacturer if you require additional information.
The official notice
This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.
Read the official notice (opens in a new tab)
United States