MAUDE Adverse Event Report: STRYKER-ENDOSCOPY PHOENIX USA; CATHETER, RECORDING, ELECTRODE, REPROCESSED

Model Number	200131
Medical Device Problem Codes	Device Damaged Prior to Receipt by User (1570); Use of Device Problem (1670); Mechanical Jam (2983)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/01/2024
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The device was returned to stryker sustainability solutions for evaluation.The complaint device was noted to be returned to stryker via an improper shipping methods, in which, likely generated handling damage to all complaints associated with the return.Upon visual inspection of the received complaint device, damage to the catheter deflection mechanism was observed.Waves were present throughout the catheter shaft when actuating the deflection mechanism, indicating internal wiring damage.No further relevant visible damage was observed.The catheter distal tip appeared to be intact.The catheter passed the curve specification, however, failed the planarity evaluation.As the complaint device was returned via improper shipping methods, it cannot be confirmed whether or not the planarity failure identified during functional inspection is the customer's reported experience or a result of shipping and handling damage.Therefore, the results of the investigation determined that the customer's reported event is not confirmed.A review of the dhr supports that the device met all inspection and test criteria prior to release from stryker.Therefore, the reported event could be attributed to: - user error (including user technique and methods).- user error (including excessive force applied to the deflection mechanism).- shipping and handling damage (including the improper return of the reported complaint device).The instructions for use (ifu) state: ¿ do not attempt to use the reprocessed ep catheter prior to completely reading and understanding the directions for use.¿ inspect the packaging and catheter for damage or defects prior to use.¿ avoid excessive torque, stretching, kinking and/or bending of catheter, as this may interfere with distal tip shaping or cause damage to internal electrode wires.¿ avoid manual pre-bending of distal curve, as this may damage steering mechanism of steerable catheters.Handle catheter with care to avoid improper electrical functioning.¿ avoid excessive contact of handpiece with fluids, as this could adversely affect the electrical performance of the catheter.¿ diagnostic ep catheters are not recommended for long-term pacing.¿ do not insert or withdraw the catheter without straightening the catheter tip.¿ this device should not be used with magnetic resonance imaging (mri) systems.¿ use fluoroscopic guidance during catheter positioning.Storage and handling: ¿ prior to use, store reprocessed ep catheters in a cool, dry, dark place.Compatibility: ¿ ep catheters are connected to standard electronic recording equipment using appropriate cable connectors.The reported event will continue to be monitored through post-market surveillance.
Event or Problem Description
It was reported that for the catheter: poor steering.There was no patient injury, medical intervention, or extended procedure time reported.These are commonly used devices that are readily available.

• Brand Name: NA
• Common Device Name: CATHETER, RECORDING, ELECTRODE, REPROCESSED
• Manufacturer (Section D): STRYKER-ENDOSCOPY PHOENIX USA; 10232 s. 51st st.; phoenix AZ 85044
• Manufacturer (Section G): STRYKER-ENDOSCOPY PHOENIX USA; 10232 s. 51st st.; phoenix AZ 85044
• Manufacturer Contact: andy dobos ; 1810 w. drake drive; tempe, AZ 85283 ; 8888883433
• MDR Report Key: 20139669
• Report Number: 0002090040-2024-00012
• Device Sequence Number: 7417024
• Product Code: NLH
• UDI-Device Identifier: 00885825002930
• UDI-Public: 00885825002930
• Combination Product (Y/N): N
• Initial Reporter State: DE
• Initial Reporter Country: US
• PMA/510(K) Number: K030187
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 09/04/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 02/09/2026
• Device Model Number: 200131
• Device Catalogue Number: 200131
• Device Lot Number: 5295104SH
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 07/22/2024
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 08/08/2024
• Initial Report FDA Received Date: 09/04/2024
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 02/09/2024
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): Yes
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown