HLS CANNULA + PIK
Report
- Report Number
- 3013876692-2025-00070
- Event Type
- Death
- Date Received
- August 18, 2025
- Date of Event
- July 10, 2025
- Report Date
- May 12, 2026
- Manufacturer
- MAQUET CARDIOPULMONARY GMBH
- Product Code
- DWF
- PMA / PMN Number
- K102532
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Distributor report
- Reporter Location
- US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Narratives
ON (B)(6) 2026, A NEW FILE AND TELEPHONE NUMBER HAS BEEN RECEIVED FROM UNI REGENSBURG (FILE NUMBER: (B)(6), TELEPHONE NUMBER: (B)(6). A FOLLOW UP MEDWATCH WILL BE SUBMITTED WHEN ADDITIONAL INFORMATION BECOMES AVAILABLE.
A PHONE CALL BETWEEN GETINGE DCU (DESIGNATED COMPLAINT UNIT) TEAM LEAD, AND THE REGENSBURG CRIMINAL INVESTIGATION DEPARTMENT (MR. (B)(6)) TOOK PLACE ON 2026-05-05 AT 14:35 PM. DURING THIS CALL MR. (B)(6) REPORTED THAT AN EXTERNAL INVESTIGATION WAS ORDERED 2026-01-29 BY AN INDEPENDENT EXPERT. THIS INVESTIGATION IS ONGOING. MR. (B)(6) WILL INFORM GETINGE AS SOON AS THE FINAL REPORT WAS RECEIVED. A FOLLOW UP MEDWATCH WILL BE SUBMITTED WHEN ADDITIONAL INFORMATION BECOMES AVAILABLE.
A PHONE CALL BETWEEN GETINGE DCU (DESIGNATED COMPLAINT UNIT) TEAM LEAD, SENIOR COMPLAINT HANDLER, AND THE PUBLIC PROSECUTOR¿S OFFICE FROM (B)(6) TOOK PLACE ON 2026-03-17 AT 14:30 PM. DURING THIS CALL, THE PERSON AT THE HOTLINE THERE CONFIRMED THE CASE NUMBER (B)(4) PROVIDED TO THE MANUFACTURER IS INCORRECT. THE SSU WAS CONTACTED ON THE SAME DAY 2026-03-17 TO REQUEST THE CORRECT CASE NUMBER AT THE HOSPITAL ASAP. NEW INFORMATION WAS PROVIDED BY THE SSU ON 2026-03-17 THAT A CONVERSATION WAS HELD WITH (B)(6) FROM THE LEGAL DEPARTMENT AT THE (B)(6) HOSPITAL AND HOSPITAL IS NOT WILLING TO SHARE THE CORRECT FILE NUMBER DUE TO ONGOING INVESTIGATIONS. THEY FURTHER INFORMED THAT GETINGE WILL BE INFORMED AS SOON AS THE INVOLVED DEVICES (ROTAFLOW/PLS/CANNULAS) HAS BEEN RELEASED. A FOLLOW UP MEDWATCH WILL BE SUBMITTED WHEN ADDITIONAL INFORMATION BECOMES AVAILABLE.
A FOLLOW UP MEDWATCH WILL BE SUBMITTED WHEN ADDITIONAL INFORMATION BECOMES AVAILABLE.
ADDITONAL INFORMATION HAS BEEN PROVIDED BY THE GETINGE SSU (SALES AND SERVICE UNIT) AS FOLLOWS: DUE TO THE PATIENT'S PRE-EXISTING MEDICAL CONDITIONS AND THE POOR PROGNOSIS THAT ALREADY EXISTED BEFORE THE INCIDENT, A CUSTOMER DECISION WAS MADE AGAINST CHANGING THE SET AND TREATMENT WAS DISCONTINUED.THE INVESTIGATION IS ONGOING. NO FURTHER INFORMATION IS AVAILABLE RIGHT NOW FOR PRODUCT INVESTIGATION. THE PRODUCTS ARE STILL CONFISCATED. ON (B)(6) 2025 THE TELEPHONE NUMBER AND THE FILE REFERENCE NUMBER (B)(4) OF THE REGENSBURG PUBLIC PROSECUTOR WAS PROVIDED BY THE SSU (SALES AND SERVICE UNIT), FURTHER COMMUNICATION WILL BE PERFORMED BY MAQUET CARDIOPULMONARY GMBH. A FOLLOW UP MEDWATCH WILL BE SUBMITTED WHEN ADDITIONAL INFORMATION BECOMES AVAILABLE.
COMPLAINT#: (B)(4).
COMPLAINT #(B)(4).
COMPLAINT # (B)(4).
IT WAS REPORTED THAT DURING PREPARATION FOR A PLANNED CT SCAN ¿ PLANNED IN-HOUSE PATIENT TRANSPORT WITH VA ECMO FROM THE INTENSIVE CARE UNIT TO THE CT ¿ THE ROTAFLOW DRIVE UNIT WAS POSITIONED IN THE PATIENT BED AS PER INSTRUCTIONS. THE DRIVE PUMP WAS RUNNING CORRECTLY AT A FLOW RATE OF 2.6 L/MIN. SUDDENLY, THE ROTAFLOW FLOW INDICATOR ALERTED, AND THE FLOW INDICATOR WAS NO LONGER READABLE. AT THE SAME TIME, A SIGNIFICANTLY LOUDER ROTATION NOISE FROM THE DRIVE PUMP WAS AUDIBLE. AN IMMEDIATE, COMPLETE INSPECTION REVEALED THAT AIR HAD ENTERED THE SYSTEM. THE ARTERIAL LINE WAS IMMEDIATELY CLAMPED, AND THE ECMO SPEED WAS COMPLETELY REDUCED. AFTER IMMEDIATELY CLAMPING THE ARTERIAL LINE AND REDUCING THE ECMO SPEED, THE PERFUSIONISTS WERE IMMEDIATELY INFORMED, WITH THE URGENT INSTRUCTION TO IMMEDIATELY TRANSFER A FILLED, READY-TO-USE SYSTEM TO THE INTENSIVE CARE UNIT. THE SUBSEQUENT INSPECTION OF THE ECMO SYSTEM TOGETHER WITH THE ATTENDING PHYSICIANS REVEALED NO VISIBLE DAMAGE TO THE ECMO. ANALYSIS: DURING THE UKR'S ANALYSIS OF THE AFFECTED PRODUCTS, NO UNDESIRABLE SIDE EFFECTS, NO MALFUNCTION, NO APPLICATION ERROR, AND NO INADEQUACY OF THE INFORMATION PROVIDED WERE IDENTIFIED. CUSTOMER MENTIONED THAT "ALTHOUGH WE HAVE EXHAUSTED OUR ANALYTICAL CAPABILITIES, WE CANNOT COMPLETELY RULE OUT THE ABOVE-MENTIONED ERROR POSSIBILITIES, AND THEREFORE WE ARE REPORTING THE FATAL PATIENT INJURY RESULTING IN DEATH". DUE TO THE POLICE INVESTIGATION, THE DISPOSABLE PRODUCTS ARE NO LONGER WITHIN OUR CONTROL. THE LOT INFORMATION FOR THE INVOLVED DISPOSABLE PRODUCTS ARE THEREFORE NOT AVAILABLE. THE OTHER HARDWARE IS SECURELY STORED AT THE UKR. AS MULTIPLE GETINGE PRODUCTS WERE USED DURING THE TREATMENT, THIS COMPLAINT WILL FOCUS ON INVESTIGATING THE SPECIFIC PRODUCT BE-PVL 2155, MATERIAL NUMBER 701047294. THE INVESTIGATION OF OTHER RELEVANT PRODUCTS WILL BE COVERED UNDER THE FOLLOWING COMPLAINT NUMBERS: BE-PAS 1515, MATERIAL NUMBER 701047280: ONETRACK #(B)(4), BE-PLS 2050, MATERIAL NUMBER 701068386: ONETRACK #(B)(4), ROTAFLOW: ONETRACK #1346851. DUE TO THE REPORTED DEATH A REPORT IS REQUIRED. COMPLAINT #(B)(4).
COMPLAINT #(B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 29985 | HLS CANNULA + PIK | CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS | DWF | MAQUET CARDIOPULMONARY GMBH | BE-PVL 2155 | UNKNOWN |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |