MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2017-12-08 for VITEK? 2 NH TEST KIT 21346 manufactured by Biomerieux, Inc.
[95743085]
A customer from (b)(6) reported to biom? Rieux a misidentification of a campylobacter jejuni ssp. Jejuni quality control sample (atcc 33560), as campylobacter coli in association with the vitek? 2 nh test kit. The customer confirmed that the strain was c. Jejuni ssp. Jejuni via maldi-tof method and offline hippurate test (positive reaction is observed; c. Jejuni ssp. Jejuni exhibits positive hippurate, while c. Coli exhibits negative hippurate). The isolate was tested with the vitek? 2 nh three times, with cultures from different media [once from cba (validated) and twice from campy agar (not validated)], and all results were given c. Coli with 99% probability. There was no patient involvement as the event pertained to a quality control sample. A biom? Rieux internal investigation will be initiated.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1950204-2017-00437 |
| MDR Report Key | 7100009 |
| Report Source | FOREIGN,HEALTH PROFESSIONAL,U |
| Date Received | 2017-12-08 |
| Date of Report | 2018-05-10 |
| Date Mfgr Received | 2018-04-17 |
| Device Manufacturer Date | 2017-06-20 |
| Date Added to Maude | 2017-12-08 |
| 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 | 3 |
| Event Location | 3 |
| Manufacturer Contact | MR. JEFF SCANLAN |
| Manufacturer Street | 595 ANGLUM ROAD |
| Manufacturer City | HAZELWOOD MO 63042 |
| Manufacturer Country | US |
| Manufacturer Postal | 63042 |
| Manufacturer Phone | 3147318694 |
| Manufacturer G1 | BIOMERIEUX, INC |
| Manufacturer Street | 595 ANGLUM ROAD |
| Manufacturer City | ST. LOUIS MO 63042 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 63042 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | VITEK? 2 NH TEST KIT |
| Generic Name | VITEK? 2 NH TEST KIT |
| Product Code | JST |
| Date Received | 2017-12-08 |
| Catalog Number | 21346 |
| Lot Number | 2450389203 |
| ID Number | 03573026144357 |
| Device Expiration Date | 2018-12-20 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BIOMERIEUX, INC |
| Manufacturer Address | 595 ANGLUM ROAD ST. LOUIS MO 63042 US 63042 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2017-12-08 |