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Recall Observatory FDA recall evidence

Device product

MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Philips Plug Style Connector, REF/Catalog Number 2602H Indicated for use in external pacing, defibrillation and monitoring applications as a non-sterile, disposable device for single pediatric use, only. The PadPro 2602 electrodes provide the conductive interface between the defibrillator and/or the external transcutaneous (non-invasive) cardiac pacemaker and the pediatric patients skin. The electrode is intended for use on pediatric infants whose weight is less than 10 kg. (22 lbs.).

Z-1176-2018

February 23, 2018

Class II

Product summary

Firm
ConMed Corporation
Event
Event 79337
Status
Terminated
Classification
Class II
Quantity
18,720 units in total
Official record key
device-enforcement:Z-1176-2018

Official wording

Reason: Wire sets of certain devices were assembled with adhesive on the contact wires, which may impede conductivity and could cause failure

Code information: Lot Numbers: Y01221601, Y03241702, Y10121501, Y020713-17, Y04071501, & Y12021501.

Distribution pattern: Worldwide Distribution: US (Nationwide) and countries of: New Zealand, Saudi Arabia, Switzerland, United Arab Emirates Uruguay & Republic of Macedonia (The former Yugoslav Republic of Macedonia).

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Wire sets of certain devices were assembled with adhesive on the contact wires, which may impede conductivity and could cause failure