MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2010-09-28 for NOT APPLICABLE N/A 445850 manufactured by Beckman Coulter Inc..
[20936555]
Beckman coulter inc. (bci) warehouse reported leaking cx triglyceride reagent due to loose caps. No injury was reported.
Patient Sequence No: 1, Text Type: D, B5
[21232235]
The incident occurred at bci warehouse.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 2050012-2010-00924 |
MDR Report Key | 1846758 |
Report Source | 05 |
Date Received | 2010-09-28 |
Date of Report | 2010-09-28 |
Date of Event | 2010-08-31 |
Date Mfgr Received | 2010-08-31 |
Device Manufacturer Date | 2010-04-16 |
Date Added to Maude | 2012-01-06 |
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 | 0 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | MS. NORA ZEROUNIAN |
Manufacturer Street | 250 S. KRAEMER BLVD |
Manufacturer City | BREA CA 92821 |
Manufacturer Country | US |
Manufacturer Postal | 92821 |
Manufacturer Phone | 7149613634 |
Manufacturer G1 | BECKMAN COULTER INC. |
Manufacturer Street | 250 S. KRAEMER BLVD. |
Manufacturer City | BREA CA 92821 |
Manufacturer Country | US |
Manufacturer Postal Code | 92821 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | NOT APPLICABLE |
Generic Name | NOT APPLICABLE |
Product Code | CDT |
Date Received | 2010-09-28 |
Model Number | N/A |
Catalog Number | 445850 |
Lot Number | N/A |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BECKMAN COULTER INC. |
Manufacturer Address | 250 S. KRAEMER BLVD BREA CA 92821 US 92821 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2010-09-28 |