Blood Pressure Module BPM3 TM-2917B (Spare Part Numbers 191378 or 191389) with firmware version S005 installed in 2008 Series Hemodialysis Machines with Part Numbers 190573, 190713, 190766, 190858, 190895, 190908, 191124, 191126, 191128, and 191130
Recall
- Recall Number
- Z-3124-2024
- Event Number
- 95169
- Firm
- Fresenius Medical Care Holdings, Inc.
- FEI Number
- 3001451489
- Product Code
- KDI
- Status
- Open, Classified
- Root Cause
- Under Investigation by firm
- Initiated
- August 8, 2024
- Posted
- September 11, 2024
- Address
- 920 Winter St, Bld 920, Waltham, MA, 02451-1521
Description
Blood Pressure Module BPM3 TM-2917B (Spare Part Numbers 191378 or 191389) with firmware version S005 installed in 2008 Series Hemodialysis Machines with Part Numbers 190573, 190713, 190766, 190858, 190895, 190908, 191124, 191126, 191128, and 191130
Machines equipped with BPM3 Blood Pressure Modules (Blood pressure monitor TM-2917B with firmware version S005) will not record Blood Pressure measurements and does not alarm if the cuff tubing is kinked close to the cuff.
An IMPORTANT MEDICAL DEVICE CORRECTION notification letter dated 8/8/24 was sent to customers. Facilities and Programs with the 2008T Hemodialysis Machine with Blood Pressure Module BPM3 should: "Visually inspect the blood pressure tubing for kinking during each monitoring and safety check. Correct any kinks if observed. "Verify visually that each scheduled blood pressure measurement was completed successfully each time period as per clinic procedures and state regulations. For further information please reference the 2008T Hemodialysis System Operator's Manual (P/N 490122 Rev. AA) https://fmcna.com/support/product-support-documents/operators-manuals-hemodialysis-hd/ Fresenius Medical Care is working diligently on a correction and will communicate when updated firmware is available. Please provide this Customer Notice to all those who need to be aware within your organization. Please complete and return the attached reply form. On 12/19/2024, Fresenius Medical sent a follow up notification letter indicating there is a new BPM3 Blood Pressure Module (firmware version S007) available that fixes this issue. Instructions included how to determine if you have affected BPM3 firmware and if it is affected, how to return the unit and order the replacement part. Customers were also instructed to notify personnel and customers, and to complete and return the response form.
US Nationwide. Canada.
3,718 systems