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

• 
  Reason
• 
  Affected products

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