MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2003-07-23 for SICKLEDEX TUBE TEST OF HEMOGLOBIN S NI 773200 manufactured by Ortho-clinical Diagnostics, Inc..
[20994092]
Customer reported that a pt with a hemoglobin s of 22%, as determined by hemoglobin electrophoresis, tested negative with this product. No reported death or serious injury was associated with this incident.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2250051-2003-00919 |
| MDR Report Key | 473989 |
| Date Received | 2003-07-23 |
| Date of Report | 2003-07-15 |
| Date of Event | 2003-07-15 |
| Date Added to Maude | 2003-07-29 |
| Event Key | 0 |
| Report Source Code | Distributor report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 0 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | SICKLEDEX TUBE TEST OF HEMOGLOBIN S |
| Generic Name | NA |
| Product Code | GHM |
| Date Received | 2003-07-23 |
| Model Number | NI |
| Catalog Number | 773200 |
| Lot Number | 1195 |
| ID Number | NA |
| Device Expiration Date | 2002-06-28 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | NA |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 462841 |
| Manufacturer | ORTHO-CLINICAL DIAGNOSTICS, INC. |
| Manufacturer Address | 1001 US HWY 202 RARITAN NJ 088690606 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2003-07-23 |