Skip to content

N/A (REF BD710FJ282CT)Recalls & reported problems

Stryker Sustainability Solutions, Inc. · Diagnostic EP Catheter FJ, 7F · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885825000271), received between Mar 10, 2025 and Mar 10, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Energy Output Problem” (1 report).

27 other recalls cover devices cleared under the same FDA submission (K100254); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 1 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Energy Output Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMar 10, 2025Energy Output Problem; Energy Output Problem

    IT WAS REPORTED THAT FOR THE CATHETER THERE WAS A BAD ELECTRODE CS 9,10. THERE WAS NO PATIENT INJURY OR MEDICAL INTERVENTION AND EXTENDED PROCEDURE TIME REPORTED WAS TWO MINUTES. THESE ARE COMMONLY USED DEVICES THAT ARE READILY AVAILABLE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21560473 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K100254. One submission often covers many models, so check the product and lot details in each record.

  • Z-2181-2026 · Apr 10, 2026 · Open, Classified
    BARD EP XT Decapolar Steerable, Product Number 201007; REPROCESSED ELECTROPHYSIOLOGY CATHETER
  • Z-2185-2026 · Apr 10, 2026 · Open, Classified
    CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER
  • Z-2186-2026 · Apr 10, 2026 · Open, Classified
    Daig Livewire Steerable, Product Number 401575; REPROCESSED ELECTROPHYSIOLOGY CATHETER
  • Z-2177-2026 · Apr 10, 2026 · Open, Classified
    BARD Dynamic Tip Steerable, Product Number 6DYNTP001;
  • Z-2196-2026 · Apr 10, 2026 · Open, Classified
    Daig Livewire Steerable, Product Number 401923; REPROCESSED ELECTROPHYSIOLOGY CATHETER
  • Z-2198-2026 · Apr 10, 2026 · Open, Classified
    Daig Livewire Steerable BDB, Product Number 401918, REPROCESSED ELECTROPHYSIOLOGY CATHETER
  • Z-2187-2026 · Apr 10, 2026 · Open, Classified
    Daig Livewire Steerable, Product Number 401581; REPROCESSED ELECTROPHYSIOLOGY CATHETER
  • Z-2183-2026 · Apr 10, 2026 · Open, Classified
    BW Webster Duo-Decapolar, Product Number D728260RT; REPROCESSED ELECTROPHYSIOLOGY CATHETER
  • Z-2174-2026 · Apr 10, 2026 · Open, Classified
    BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER
  • Z-2176-2026 · Apr 10, 2026 · Open, Classified
    BARD Dynamic Tip Steerable, Product Number 200344; REPROCESSED ELECTROPHYSIOLOGY CATHETER
  • Z-2197-2026 · Apr 10, 2026 · Open, Classified
    Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER
  • Z-2182-2026 · Apr 10, 2026 · Open, Classified
    BARD EP XT Steerable, Product Number 200794; REPROCESSED ELECTROPHYSIOLOGY CATHETER
  • Z-2194-2026 · Apr 10, 2026 · Open, Classified
    Daig Livewire Steerable, Product Number 401914; REPROCESSED ELECTROPHYSIOLOGY CATHETER
  • Z-2193-2026 · Apr 10, 2026 · Open, Classified
    Daig Livewire Steerable, Product Number 401908; REPROCESSED ELECTROPHYSIOLOGY CATHETER
  • Z-2188-2026 · Apr 10, 2026 · Open, Classified
    Daig Livewire Steerable, Product Number 401582; REPROCESSED ELECTROPHYSIOLOGY CATHETER

…and 12 more.

Other CATHETER, RECORDING, ELECTRODE, REPROCESSED devices

All CATHETER, RECORDING, ELECTRODE, REPROCESSED devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.