MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2015-12-01 for ARCHITECT I2000SR ANALYZER 03M74-97 manufactured by Abbott Manufacturing Inc.
[32453209]
Patient identifier did not contain enough spaces for entire id. The entire id is (b)(6). (b)(4). A followup report will be submitted when the evaluation is complete. Evaluation in process.
Patient Sequence No: 1, Text Type: N, H10
[32453210]
The account generated repeatedly reactive architect hiv ag/ab combo results on a post-mortem sample id (b)(6) that tested nonreactive on another architect analyzer. The sample was also negative with western blot and rna testing. The post mortem sample was screened for bone transplantation. Bones, tissues and other transplantation materials were lost due to the (b)(6). No specific donor information is known. No impact to recipients was reported.
Patient Sequence No: 1, Text Type: D, B5
[40984434]
Additional information was provided during evaluation: (b)(6) architect hiv ag/ab combo results were also obtained on a third architect instrument by using the same reagent lots. This instrument is utilized for clinical studies performed and managed by an abbott clinical studies coordinator. The two post mortem samples were run on this architect instrument for troubleshooting purposes only. No issues were observed with "normal" samples or controls performed on the three architect i2000sr analyzers. An evaluation was performed for both the architect i2000sr analyzer and reagent lots. Architect hiv ag/ab combo evaluation: a review of the product labeling concluded that the issue is sufficiently addressed. The tracking and trending report review determined that there are no related adverse or non-statistical trends for the reagent lots involved in this event and no non-conformances and deviations associated with the affected reagent lots have been identified. A retained reagent kit of lot 54325li00 was tested in a specificity and sensitivity setup. Results of this setup did not implicate that the specificity or sensitivity performance of the lot is negatively impacted. The reagent kit showed normal performance without (b)(6) results. Additionally, the specificity performance were tested with lot 53118li00 and no (b)(6) results were obtained. Based on this data, the performance of the architect hiv ag/ab combo reagent lot 53110li00 and 54325li00 is acceptable. Architect i2000sr evaluation: the field service engineer (fse) proactively cleaned and replaced several parts on the architect i2000sr. No subsequent occurrences of (b)(6) results were documented after the part replacements and cleaning of the optics. A review of the architect isr05922 service history was performed. No additional contributing factors on or around the date of the event were identified, and no subsequent occurrences of (b)(6) results were found after the cleaning of the optics and replacement of multiple parts by the fse. The architect system operations manual addresses operational precautions and limitations and addresses probable causes and corrective actions for the troubleshooting of (b)(6) results. A review of the architect product monitoring review found no similar issues as described in this complaint, and no trend associated with the architect i2000sr erratic result rate was identified. Based on the available information, there is insufficient evidence to reasonably suggest a malfunction of the architect i2000sr. The evaluation did not identify a specific reason, why the customer experienced this problem, but a possible explanation may be that the (b)(6) results were due to sample integrity issues or due to the colour (almost black) of the affected samples. According to the package insert of the assay an important factor to obtain consistency in results is the quality of the sample. Based on this data, it is concluded that the architect hiv ag/ab combo reagent lots, identified in this complaint are performing acceptably, and there is no indication of a deficiency of the architect i2000sr or the various i2000sr parts replaced and/or cleaned.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 1628664-2015-00310 |
| MDR Report Key | 5258612 |
| Report Source | FOREIGN,HEALTH PROFESSIONAL |
| Date Received | 2015-12-01 |
| Date of Report | 2016-02-24 |
| Date of Event | 2015-10-19 |
| Date Mfgr Received | 2016-02-05 |
| Date Added to Maude | 2015-12-01 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 0 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | NOEMI ROMERO-KONDOS, RN BSN |
| Manufacturer Street | 100 ABBOTT PARK ROAD DEPT. 09B9, LCCP1-3 |
| Manufacturer City | ABBOTT PARK IL 600643537 |
| Manufacturer Country | US |
| Manufacturer Postal | 600643537 |
| Manufacturer Phone | 224667-512 |
| Manufacturer G1 | ABBOTT MANUFACTURING INC |
| Manufacturer Street | 1921 HURD DRIVE |
| Manufacturer City | IRVING TX 75038 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 75038 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ARCHITECT I2000SR ANALYZER |
| Generic Name | AUTOMATED IMMUNOASSAY ANALYZER |
| Product Code | NHS |
| Date Received | 2015-12-01 |
| Catalog Number | 03M74-97 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | DA |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 0 |
| Device Event Key | 0 |
| Manufacturer | ABBOTT MANUFACTURING INC |
| Manufacturer Address | 1921 HURD DRIVE IRVING TX 75038 US 75038 |
| Brand Name | ARCHITECT I2000SR ANALYZER |
| Generic Name | AUTOMATED IMMUNOASSAY ANALYZER |
| Product Code | JJE |
| Date Received | 2015-12-01 |
| Catalog Number | 03M74-97 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | DA |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ABBOTT MANUFACTURING INC |
| Manufacturer Address | 1921 HURD DRIVE IRVING TX 75038 US 75038 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Deathisabilit | 2015-12-01 |