MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,other report with the FDA on 2015-10-10 for BLOOD COLLECTION DEVICE MBC6000 manufactured by Carefusion.
[28033562]
Although requested, the affected product has not been received. A follow up report will be submitted with investigation results should the devices be received for evaluation.
Patient Sequence No: 1, Text Type: N, H10
[28033564]
The customer reported that the rubber stopper that covers the needle is separating from the blood collection tube holder. There was no patient harm reported.
Patient Sequence No: 1, Text Type: D, B5
[45484231]
Patient Sequence No: 1, Text Type: N, H10
Report Number | 9616066-2015-01247 |
MDR Report Key | 5142487 |
Report Source | COMPANY REPRESENTATIVE,OTHER |
Date Received | 2015-10-10 |
Date of Report | 2015-10-01 |
Date Mfgr Received | 2016-04-22 |
Device Manufacturer Date | 2015-03-10 |
Date Added to Maude | 2015-10-10 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR. ADE AJIBADE |
Manufacturer Street | 10020 PACIFIC MESA BLVD |
Manufacturer City | SAN DIEGO CA 921214386 |
Manufacturer Country | US |
Manufacturer Postal | 921214386 |
Manufacturer Phone | 8586172000 |
Manufacturer G1 | CAREFUSION |
Manufacturer Street | 10020 PACIFIC MESA BLVD |
Manufacturer City | SAN DIEGO CA 921214386 |
Manufacturer Country | US |
Manufacturer Postal Code | 921214386 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | BLOOD COLLECTION DEVICE |
Generic Name | BLOOD COLLECTION |
Product Code | KST |
Date Received | 2015-10-10 |
Model Number | MBC6000 |
Catalog Number | MBC6000 |
Lot Number | 301150310 |
Device Expiration Date | 2018-03-01 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CAREFUSION |
Manufacturer Address | 10020 PACIFIC MESA BLVD SAN DIEGO CA 921214386 US 921214386 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2015-10-10 |