MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2013-03-08 for VITROS CHEMISTRY PRODUCTS PHBR SLIDES 8221384 manufactured by Ortho-clinical Diagnostics.
[3134492]
The customer obtained multiple, non-reproducible, lower than expected vitros phbr quality control results using a vitros 5600 integrated system. Qc fluid lot biorad 3 = 33. 9 vs. Expected result = 52. 88 ng/ml; qc fluid lot g1647 = 7. 8, 8. 1, 8. 2 vs. Expected result = 11. 89 ng/ml; qc fluid lot q2098 = 48. 0, 48. 0, 49. 0 vs. An expected result= 63. 57 ng/ml; biased results of the direction and magnitude observed may lead to inappropriate physician action if they were to occur undetected on patient samples. No patient samples were run for vitros phbr during the time frame of the event. There was no report of patient harm as a result of this event. This report is number one of seven mdr's for this event. Seven 3500a forms are being submitted for this event as seven devices were involved. (b)(4).
Patient Sequence No: 1, Text Type: D, B5
[10522748]
The investigation confirmed that multiple, non-reproducible, lower than expected vitros phbr quality control results were predicted while using the vitros 5600 integrated system. The investigation concludes that the affected results were associated with the use of an atypical phbr calibration. The specific cause of the atypical calibration is unknown. However, a reagent related issue cannot be ruled out as a contributing factor. Expected vitros phbr quality control results were obtained upon recalibrating the same reagent lot. There is no evidence that an instrument related issue contributed to the event. No service actions were performed. Additional investigation by ocd regarding vitros phbr reagent is ongoing.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 1319809-2013-00099 |
| MDR Report Key | 2995407 |
| Report Source | 05 |
| Date Received | 2013-03-08 |
| Date of Report | 2013-03-08 |
| Date of Event | 2013-02-12 |
| Date Mfgr Received | 2013-02-12 |
| Device Manufacturer Date | 2012-12-20 |
| Date Added to Maude | 2013-05-14 |
| 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 |
| Reporter Occupation | MEDICAL TECHNOLOGIST |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Manufacturer Contact | MR. JOSEPH FALVO |
| Manufacturer Street | 100 INDIGO CREEK DRIVE |
| Manufacturer City | ROCHESTER NY 14626 |
| Manufacturer Country | US |
| Manufacturer Postal | 14626 |
| Manufacturer Phone | 5854533000 |
| Manufacturer G1 | ORTHO-CLINICAL DIAGNOSTICS |
| Manufacturer Street | 100 INDIGO CREEK DRIVE |
| Manufacturer City | ROCHESTER NY 14626 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 14626 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | VITROS CHEMISTRY PRODUCTS PHBR SLIDES |
| Generic Name | IN-VITRO DIAGNOSTIC |
| Product Code | DLZ |
| Date Received | 2013-03-08 |
| Catalog Number | 8221384 |
| Lot Number | 2540-0063-0274 |
| Device Expiration Date | 2013-12-01 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ORTHO-CLINICAL DIAGNOSTICS |
| Manufacturer Address | 100 INDIGO CREEK DRIVE ROCHESTER NY 14626 US 14626 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2013-03-08 |