N/A (REF 201106)Recalls & reported problems
Stryker Sustainability Solutions, Inc. · Steerable Diagnostic EP Catheter , LARGE 4.0, 8 electrodes, 2mm spacing, 6F · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 00885825003920), received between Sep 27, 2017 and Sep 27, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Defective Device” (1 report).
28 other recalls cover devices cleared under the same FDA submission (K030187); 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.
Most reported problems
Device problems
- Defective Device1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 27, 2017Defective Device; Defective Device
IT WAS REPORTED THAT THE SHAPE OF THE ELECTROPHYSIOLOGY CATHETER WAS NOT CORRECT. MULTIPLE ATTEMPTS WERE MADE TO OBTAIN ADDITIONAL INFORMATION. NO INFORMATION WAS PROVIDED. HOWEVER, THERE WAS NO PATIENT INJURY, MEDICAL INTERVENTION, OR EXTENDED PROCEDURE TIME REPORTED. THESE ARE COMMONLY USED DEVICES THAT ARE READILY AVAILABLE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6899088 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K030187. One submission often covers many models, so check the product and lot details in each record.
- Z-0085-2027 · Aug 18, 2026 · Open, ClassifiedBARD EP XT DECAPOLAR STEERABLE, DIAGNOSTIC EP CATHETER, 6F, LARGE 4.0, 10, 2-5-2MM, REF: 201007
- Z-2176-2026 · Apr 10, 2026 · Open, ClassifiedBARD Dynamic Tip Steerable, Product Number 200344; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2179-2026 · Apr 10, 2026 · Open, ClassifiedBARD Dynamic XT Steerable, Product Number 201103, REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2191-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2182-2026 · Apr 10, 2026 · Open, ClassifiedBARD EP XT Steerable, Product Number 200794; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2178-2026 · Apr 10, 2026 · Open, ClassifiedBARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2192-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable, Product Number 401905; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2199-2026 · Apr 10, 2026 · Open, ClassifiedMedtronic Marinr Steerable, Product Number 72402; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2187-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable, Product Number 401581; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2177-2026 · Apr 10, 2026 · Open, ClassifiedBARD Dynamic Tip Steerable, Product Number 6DYNTP001;
- Z-2184-2026 · Apr 10, 2026 · Open, ClassifiedCS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2175-2026 · Apr 10, 2026 · Open, ClassifiedBARD Dynamic Tip Steerable, Product Number 200131; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2197-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2180-2026 · Apr 10, 2026 · Open, ClassifiedBARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2190-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable, Product Number 401652; REPROCESSED ELECTROPHYSIOLOGY CATHETER
…and 13 more.
Other CATHETER, RECORDING, ELECTRODE, REPROCESSED devices
- MEDLINE 401904RHMedline Industries, Inc. · Catheter, recording, electrode, reprocessed3 recalls1 report
- MEDLINE 401582RHMedline Industries, Inc. · Catheter, recording, electrode, reprocessed3 recalls0 reports
- MEDLINE 401474RHMedline Industries, Inc. · Catheter, recording, electrode, reprocessed2 recalls1 report
- MEDLINE 81102RHMedline Industries, Inc. · Catheter, recording, electrode, reprocessed2 recalls0 reports
- MEDLINE BD710FJ282RRHMedline Industries, Inc. · Catheter, recording, electrode, reprocessed2 recalls0 reports
- MEDLINE BD710DF282RRHMedline Industries, Inc. · Catheter, recording, electrode, reprocessed2 recalls0 reports
- MEDLINE 401448RHMedline Industries, Inc. · Catheter, recording, electrode, reprocessed2 recalls0 reports
- MEDLINE 401222RHMedline Industries, Inc. · Catheter, recording, electrode, reprocessed2 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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