MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2016-06-17 for CLINIMACS TUBING SET LS N/A 162-01 manufactured by Miltenyi Biotec Gmbh.
[47621319]
Patient Sequence No: 1, Text Type: N, H10
[47621320]
The customer reported that one of their clinimacs tubing sets ls had a leak during priming and as a consequence the process stopped. The cellular product was not affected and a replacement tubing set was used to finish the cell separation procedure. Any risk for the patient's therapy could be therefore ruled out.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3005290010-2016-00072 |
MDR Report Key | 5732464 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2016-06-17 |
Date of Report | 2016-06-16 |
Date of Event | 2016-04-26 |
Date Mfgr Received | 2016-05-18 |
Device Manufacturer Date | 2015-12-22 |
Date Added to Maude | 2016-06-17 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS NANCY JOHANSEN |
Manufacturer Street | 85 HAMILTON ST |
Manufacturer City | CAMBRIDGE MA 02139 |
Manufacturer Country | US |
Manufacturer Postal | 02139 |
Manufacturer Phone | 6172180062 |
Manufacturer G1 | MILTENYI BIOTEC GMBH |
Manufacturer Street | FRIEDRICH-EBERT-STRASSE 68 |
Manufacturer City | BERGISCH GLADBACH, 51429 |
Manufacturer Country | GM |
Manufacturer Postal Code | 51429 |
Single Use | 3 |
Remedial Action | RL |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CLINIMACS TUBING SET LS |
Generic Name | CLINIMACS TUBING SET LS |
Product Code | OVG |
Date Received | 2016-06-17 |
Model Number | N/A |
Catalog Number | 162-01 |
Lot Number | B2534 |
Device Expiration Date | 2018-07-10 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MILTENYI BIOTEC GMBH |
Manufacturer Address | FRIEDRICH-EBERT-STRASSE 68 BERGISCH GLADBACH, 51429 GM 51429 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2016-06-17 |