MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2007-04-17 for DRIED POS COMBO TYPE 20 B1017-200 manufactured by Dade Behring, Inc..
[17399026]
Customer reported s. Aureus isolate oxacillin (ox) mic discrepancy. They obtained oxacillin-susceptible results on the dried pos combo type 20 panel and oxacillin-resistant results on secondary methods that were also performed for the clinical isolate. Results were reported to the physician. Pt treatment was not prescribed or altered and there was no report of adverse health consequences associated with the discrepant result being obtained.
Patient Sequence No: 1, Text Type: D, B5
[17639206]
Evaluation codes: method; routine monitoring of complaint history and performance trends to ensure performance is within claims. Results: clinical isolated has not yet been received from the customer. Conclusions: clinical isolate testing is pending. Overall oxacillin performance of dried pos panels is acceptable. The cause of the failure is unk.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 2919016-2007-00001 |
| MDR Report Key | 952498 |
| Report Source | 05 |
| Date Received | 2007-04-17 |
| Date of Report | 2007-04-17 |
| Date of Event | 2007-04-04 |
| Date Mfgr Received | 2007-04-04 |
| Device Manufacturer Date | 2006-12-01 |
| Date Added to Maude | 2007-11-26 |
| 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 | OTHER HEALTH CARE PROFESSIONAL |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 0 |
| Manufacturer Contact | RICH LAGUNA |
| Manufacturer Street | 2040 ENTERPRISE BLVD |
| Manufacturer City | WEAT SACRAMENTO CA 95691 |
| Manufacturer Country | US |
| Manufacturer Postal | 95691 |
| Manufacturer Phone | 9163743163 |
| Manufacturer G1 | * |
| Manufacturer Street | * |
| Manufacturer City | * |
| Manufacturer Country | * |
| Single Use | 3 |
| Previous Use Code | 3 |
| Removal Correction Number | NA |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | DRIED POS COMBO TYPE 20 |
| Generic Name | ANTIMICROBIC SUSCEPT. TEST PANELS: GRAM POS. |
| Product Code | LTT |
| Date Received | 2007-04-17 |
| Model Number | NA |
| Catalog Number | B1017-200 |
| Lot Number | 2007-12-28 |
| ID Number | NA |
| Device Expiration Date | 2007-12-28 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | NA |
| Device Eval'ed by Mfgr | R |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 923281 |
| Manufacturer | DADE BEHRING, INC. |
| Manufacturer Address | 2040 ENTERPRISE BLVD. WEST SACRAMENTO CA 95691 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2007-04-17 |