N/A (REF 401908)Recalls & reported problems
Stryker Sustainability Solutions, Inc. · Steerable Diagnostic EP Catheter Medium Curl, 7F · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885825007287), received between Aug 1, 2018 and Aug 1, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Positioning Problem” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
25 other recalls cover devices cleared under the same FDA submission (K052603); 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-2193-2026 · Root cause: Process control · FDA record ↗
Most reported problems
Device problems
- Positioning Problem1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 1, 2018Positioning Problem; Positioning Problem
IT WAS REPORTED THE PHYSICIAN WAS UNABLE TO STEER THE ELECTROPHYSIOLOGY CATHETER. THERE WAS NO PATIENT INJURY, MEDICAL INTERVENTION, OR EXTENDED PROCEDURE TIME REPORTED. THESE ARE COMMONLY USED DEVICES THAT ARE READILY AVAILABLE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7739706 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K052603. One submission often covers many models, so check the product and lot details in each record.
- Z-2174-2026 · Apr 10, 2026 · Open, ClassifiedBARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2187-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable, Product Number 401581; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2176-2026 · Apr 10, 2026 · Open, ClassifiedBARD Dynamic Tip Steerable, Product Number 200344; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2184-2026 · Apr 10, 2026 · Open, ClassifiedCS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2188-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable, Product Number 401582; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2189-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable, Product Number 401603, REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2198-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable BDB, Product Number 401918, REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2190-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable, Product Number 401652; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2182-2026 · Apr 10, 2026 · Open, ClassifiedBARD EP XT Steerable, Product Number 200794; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2179-2026 · Apr 10, 2026 · Open, ClassifiedBARD Dynamic XT Steerable, Product Number 201103, REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2194-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable, Product Number 401914; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2199-2026 · Apr 10, 2026 · Open, ClassifiedMedtronic Marinr Steerable, Product Number 72402; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2175-2026 · Apr 10, 2026 · Open, ClassifiedBARD Dynamic Tip Steerable, Product Number 200131; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2180-2026 · Apr 10, 2026 · Open, ClassifiedBARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2186-2026 · Apr 10, 2026 · Open, ClassifiedDaig Livewire Steerable, Product Number 401575; REPROCESSED ELECTROPHYSIOLOGY CATHETER
…and 10 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.