SPS-1

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-02-02 for SPS-1 manufactured by Organ Recovery Systems.

Event Text Entries

[66669315] Pt received a kidney transplant on (b)(6) 2016 that was presented in sps solution. Pt ended up with a fungal infection that resulted in losing the transplanted kidney. Reports to this facility stated that the sps solution was contaminated: "brief summary of report: cdc, hrsa, and fda are investigating bacterial contamination of sps-1, an organ preservation solution distributed by organ recovery systems (ors). Description: this is an update to an epi-x posted on (b)(6) 2017, which reported potential bacterial contamination in sps-1 lots pbr-0074-337, pbr-0060-386, pbr-0074-330, and pbr-0060-392. Fda's investigation of potential contamination of several lots of sps-1, manufactured by organ recovery systems (ors) is ongoing. We recommend that organ procurement organizations (opo) and transplant facilities should consider transitioning to alternate, fda-cleared organ preservation fluid products from other mfrs. "
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5067658
MDR Report Key6303355
Date Received2017-02-02
Date of Report2017-02-02
Date of Event2016-08-28
Date Added to Maude2017-02-06
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag0
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSPS-1
Generic NameSPS-1
Product CodeKDN
Date Received2017-02-02
Device AvailabilityN
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerORGAN RECOVERY SYSTEMS


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Other 2017-02-02

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