Philips HEARTSTART Multifunction Electrode Pads Part Number: M3718A
Reported: October 22, 2014 Initiated: September 18, 2014 #Z-0048-2015
Product Description
Philips HEARTSTART Multifunction Electrode Pads Part Number: M3718A
Reason for Recall
Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs
Details
- Recalling Firm
- Covidien LLC
- Units Affected
- 151,210 pairs
- Distribution
- Worldwide Distribtion-USA (nationwide) including Puerto Rico and the countries of Canada Greece Israel Belgium Finland France Germany Great Britain Ireland Italy Norway Poland Portugal Spain Sweden Switzerland Brazil Chile Philippines Taiwan Australia New Zealand.
- Location
- Mansfield, MA
Frequently Asked Questions
What product was recalled? ▼
Philips HEARTSTART Multifunction Electrode Pads Part Number: M3718A. Recalled by Covidien LLC. Units affected: 151,210 pairs.
Why was this product recalled? ▼
Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 22, 2014. Severity: Critical. Recall number: Z-0048-2015.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11