N/A (REF D135304)Recalls & reported problems
Stryker Sustainability Solutions, Inc. · Diagnostic EP Catheter F Curve, 6F · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
26 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.
Recalls naming this device
- Apr 10, 2026Open, Classified
Incomplete seals on sterile product
Z-2185-2026 · Root cause: Process control · FDA record ↗
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-2197-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2191-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2184-2026 · Apr 10, 2026 · Open, ClassifiedCS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2176-2026 · Apr 10, 2026 · Open, ClassifiedBARD Dynamic Tip Steerable, Product Number 200344; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2190-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable, Product Number 401652; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2179-2026 · Apr 10, 2026 · Open, ClassifiedBARD Dynamic XT Steerable, Product Number 201103, REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2174-2026 · Apr 10, 2026 · Open, ClassifiedBARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2183-2026 · Apr 10, 2026 · Open, ClassifiedBW Webster Duo-Decapolar, Product Number D728260RT; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2178-2026 · Apr 10, 2026 · Open, ClassifiedBARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2177-2026 · Apr 10, 2026 · Open, ClassifiedBARD Dynamic Tip Steerable, Product Number 6DYNTP001;
- Z-2198-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable BDB, Product Number 401918, REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2181-2026 · Apr 10, 2026 · Open, ClassifiedBARD EP XT Decapolar Steerable, Product Number 201007; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2187-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable, Product Number 401581; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2196-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable, Product Number 401923; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2192-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable, Product Number 401905; REPROCESSED ELECTROPHYSIOLOGY CATHETER
…and 11 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.