MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05 report with the FDA on 2011-05-03 for SYNCHRON? CX AST REAGENT KIT N/A 442665 manufactured by Beckman Coulter Inc..
[1949357]
A customer contacted beckman coulter, inc. (bci), stating that the customer received a synchron cx ast reagent kit, which was cracked open. No injury or operator exposure was reported for this event.
Patient Sequence No: 1, Text Type: D, B5
[9044852]
A replacement kit was sent to the customer.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 2050012-2011-01391 |
| MDR Report Key | 2075817 |
| Report Source | 01,05 |
| Date Received | 2011-05-03 |
| Date of Report | 2011-04-05 |
| Date of Event | 2011-04-05 |
| Date Mfgr Received | 2011-04-05 |
| Device Manufacturer Date | 2010-10-28 |
| Date Added to Maude | 2011-06-13 |
| 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 | 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 BOULEVARD |
| 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? CX AST REAGENT KIT |
| Generic Name | CX AST REAGENT |
| Product Code | CKA |
| Date Received | 2011-05-03 |
| Model Number | N/A |
| Catalog Number | 442665 |
| Lot Number | T010139 |
| Device Expiration Date | 2012-04-30 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BECKMAN COULTER INC. |
| Manufacturer Address | 250 S KRAEMER BOULEVARD BREA CA 92821 US 92821 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2011-05-03 |