Health product recall

ZOLL Pro-padz Liquid Gel Radiolucent Electrodes (2019-05-27)

Starting date:
May 27, 2019
Posting date:
June 28, 2019
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-70303

Last updated: 2019-06-28

Affected Products

ZOLL Pro-padz Liquid Gel Radiolucent Electrodes

Reason

ZOLL Medical is notifying recipients of ZOLL Pro-Padz Liquid Gel Radiolucent Electrodes that some of the electrodes from lot numbers 1719, 1719A and 1819 may have been assembled incorrectly. There is no visual indication to the end user on the electrodes that the product is not assembled correctly. However, the improperly assembled electrodes will cause the defibrillator to display a "check pads" or "pads off" message and prevent the defibrillator from delivering therapy.

Affected products

ZOLL Pro-padz Liquid Gel Radiolucent Electrodes

Lot or serial number

1719
1719A
1819

Model or catalog number

8900-2105-01
8900-2106-01

Companies
Manufacturer

Zoll Medical Corporation

269 Mill Road

Chelmsford

01824

Massachusetts

UNITED STATES