MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2016-07-20 for CLINIMACS? TUBING SET LS N/A 162-01 manufactured by Miltenyi Biotec Gmbh.
[49980253]
Patient Sequence No: 1, Text Type: N, H10
[49980254]
The customer reported that the clinimacs tubing set ls spike broke at the bubble trap during usage. They informed miltenyi biotec inc. Representative which supported the customer to connect a new spike in a sterile way, so that the cells could be processed as usual.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3005290010-2016-00077 |
MDR Report Key | 5808561 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2016-07-20 |
Date of Report | 2016-07-19 |
Date of Event | 2016-06-24 |
Date Mfgr Received | 2016-06-24 |
Device Manufacturer Date | 2016-02-15 |
Date Added to Maude | 2016-07-20 |
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 | NO |
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 | 2016-07-20 |
Model Number | N/A |
Catalog Number | 162-01 |
Lot Number | B2538 |
Device Expiration Date | 2018-10-10 |
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 | 2016-07-20 |