MAUDE Adverse Event Report: THERAKOS DEVELOPMENT LIMITED CELLEX PHOTOPHERESIS SYSTEM

Catalog Number	CLXSP-I
Medical Device Problem Code	Fluid/Blood Leak (1250)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/09/2026
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The system was used for treatment.This case is reportable as a mdr due to the reportable malfunction centrifuge bowl leak/break.Since this reportable malfunction is only associated with the kit, this mdr will be only against the kit.The customer complaint investigation was performed based on the customer description and the service performed.The service technician replaced the centrifuge leak detector strip and readjusted the zero-point of the centrifuge.A device history record (dhr) review did not result in any related non-conformance's.This kit lot passed all lot release testing.A review of kit lot: p117 shows no trends.Trends were reviewed for the complaint category centrifuge bowl leak/break, and no trends were detected for this complaint category.The complaint kit was not available for evaluation.The root cause of the centrifuge bowl leak/break could not be determined.No further action is required at this time; this investigation is now complete.(b)(4).(b)(6) on (b)(6) 2026.
Event or Problem Description
The customer contacted therakos to report they experienced a centrifuge bowl break with their cellex photopheresis kit ("kit") during an extracorporeal photopheresis (ecp) treatment.Approximately 100 ml of whole blood had been processed.The customer reported that the bowl had been installed properly without issues and that no other alarms had occurred.The treatment was aborted and started again with another device.The patient was reported to be stable.There was no report of patient harm associated with this event.No product was returned for evaluation.

• Brand Name: CELLEX PHOTOPHERESIS SYSTEM
• Common Device Name: CELLEX PHOTOPHERESIS SYSTEM
• Manufacturer (Section D): THERAKOS DEVELOPMENT LIMITED; blanchardstown, dublin D15 A P2D; EI D15 AP2D
• Manufacturer (Section G): HARMAC MEDICAL PRODUCTS, INC.; 2201 bailey ave.; buffalo NY 14211
• Manufacturer Contact: mark wendelken ; 440 route 22 east; suite 302; bridgewater, NJ 08807
• MDR Report Key: 24903575
• Report Number: 3036773437-2026-00032
• Device Sequence Number: 13230134
• Product Code: LNR
• UDI-Device Identifier: 00705030000005
• UDI-Public: (01)00705030000005(10)P117(17)270301
• Combination Product (Y/N): Y
• Initial Reporter Country: SZ
• PMA/510(K) Number: P860003
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional
• Initial Reporter Occupation: Nurse
• Type of Report: Initial
• Report Date (Section B): 04/16/2026

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 Catalogue Number: CLXSP-I
• Device Lot Number: P117
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 02/09/2026
• Initial Report FDA Received Date: 04/16/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 03/18/2025
• 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): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown