MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2010-12-29 for SYNCHRON? HDLD CHOLESTEROL REAGENT 650207 (FOR REAGENT PACK) manufactured by Beckman Coulter Inc..
[1747941]
It was discovered in the beckman coulter inc. (bci) warehouse that the hdl cholesterol reagent had a broken cartridge which leaked. No injury was reported.
Patient Sequence No: 1, Text Type: D, B5
[8810151]
No additional information is available for this event.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 2050012-2010-01727 |
| MDR Report Key | 1941265 |
| Report Source | 05 |
| Date Received | 2010-12-29 |
| Date of Report | 2010-12-07 |
| Date of Event | 2010-12-07 |
| Date Mfgr Received | 2010-12-07 |
| Device Manufacturer Date | 2010-09-13 |
| Date Added to Maude | 2011-06-07 |
| 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 BOULEVARD |
| 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 |
| Removal Correction Number | NA |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | SYNCHRON? HDLD CHOLESTEROL REAGENT |
| Generic Name | HDL CHOLESTEROL REAGENT |
| Product Code | LBS |
| Date Received | 2010-12-29 |
| Model Number | NA |
| Catalog Number | 650207 (FOR REAGENT PACK) |
| Lot Number | M009386 |
| 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 | 2010-12-29 |