IMMULITE 2000 WHITE ASH
Received Aug 4, 2017 · Event occurred Jul 12, 2017
Report 2432235-2017-00464 · MDR key 6768821
Device
Generic name
Immulite 2000 White Ash
Manufacturer
Siemens Healthcare Diagnostics Products, LimitedModel number
IMMULITE 2000 WHITE ASHCatalog number
T15L2
Lot number
601
Product problems
- Adverse Event Without Identified Device or Use Problem
- Adverse Event Without Identified Device or Use Problem
Patient
Not reported
- No Known Impact Or Consequence To Patient
- No Known Impact Or Consequence To Patient
Narrative
Additional Manufacturer Narrative
THE INITIAL MDR 2432235-2017-00464 WAS FILED ON AUGUST 4TH, 2017. ADDITIONAL INFORMATION (09/27/2017): THE SIEMENS HEADQUARTER SUPPORT CENTER (HSC) GROUP PERFORMED AN INTERNAL COMPARISON BETWEEN SIEMENS T15 ASH ALLERGEN (FRAXINUS AMERICANA) AND SIEMENS A482 NOLE E1 ALLERGEN WITH 40 SAMPLES. A 2X2 CROSS TABLE EVALUATION TO COMPARE (QUALITATIVELY) THE POSITIVES AND NEGATIVES SHOWS AN OVERALL AGREEMENT OF 77.5% BETWEEN SIEMENS T15 AND A482 ALLERGENS. THE SIEMENS T15 ALLERGEN IS FAXINUS AMERICANA. THE OLE E1 HOMOLOGUE FOUND IN ASH, AS CITED IN LITERATURE, IS FRA E1 (FRAXINUS EXCELSIOR). THE IMMUNOCAP TEST CARRIES BOTH TYPES OF ASH ALLERGENS - FAXINUS AMERICANA AND FRAXINUS EXCELSIOR. AN ARTICLE "CROSS-REACTIVITY BETWEEN OLIVE AND OTHER SPECIES. ROLES OF OLE E1-RELATED PROTEIN." BY LOMBARDERO, OBISPO, CALABOZO, LEZAUN AND BARBER, DISCUSSES THE OLIVE POLLEN (OLE E1) CROSS REACTIVITY AMONG RELATED POLLENS, INCLUDING FRAXINUS EXCELSIOR. IN ADDITION, THE ARTICLE DISCUSSES A STUDY PERFORMED WHERE THE PREVALENCE OF FRA E1 IN ASH SENSITIVE INDIVIDUALS WAS ABOUT 80% IN A POPULATION THAT WAS NOT EXPOSED TO OLIVE TREES VERSUS 50% IN POPULATIONS OF MULTIPLE POLLEN ALLERGY OR EXPOSURE. BASED ON THIS STUDY, THE RATE OF CROSS REACTIVITY CAN VARY DEPENDING ON THE POPULATION TESTED AND THE EXPOSURE TO ONE OR MULTIPLE POLLENS. THE RATE OF CROSS-REACTIVITY BETWEEN THE SIEMENS T15 AND A482 ALLERGENS APPEARS TO BE ALIGNED WITH THE STUDY IN THE ARTICLE. THE SIEMENS T15 AND A482 ALLERGENS ARE PERFORMING AS EXPECTED. THE RESULT CODE AND CONCLUSION CODE HAVE BEEN UPDATED WITH THIS INFORMATION. THE CAUSE OF THE DISCORDANT FALSE NEGATIVE RESULT WITH THE T15 ALLERGEN IS UNKNOWN. NO FURTHER EVALUATION OF THE DEVICE IS REQUIRED.
Additional Manufacturer Narrative
A SIEMENS CUSTOMER CARE CENTER (CCC) SPECIALIST STATED THAT THE CUSTOMER WILL BE TESTING ALL SAMPLES ON THE A482 ALLERGEN IN ADDITION TO THE T15 ALLERGEN. THE CAUSE OF THE DISCORDANT FALSE NEGATIVE RESULT WITH THE T15 ALLERGEN IS UNKOWN. SIEMENS IS INVESTIGATING THE ISSUE. MDR 2432235-2017-00461, MDR 2432235-2017-00462 AND MDR 2432235-2017-00463 HAVE BEEN FILED FOR THE SAME ISSUE.
Description of Event or Problem
A DISCORDANT, FALSE NEGATIVE RESULT WAS OBTAINED FOR T15 ALLERGEN (WHITE ASH ALLERGEN) WITH THE IMMULITE 2000 3GALLERGY SPECIFIC IGE ASSAY ON AN IMMULITE 2000 XPI INSTRUMENT ON (B)(6) 2017. THE SAMPLE WAS RE-TESTED WITH THE IMMULITE 2000 A482 ALLERGEN (NOLE E-1 ALLERGEN) ON THE SAME INSTRUMENT AND RESULTED POSITIVE. THE INITIAL RESULT WITH T15 ALLERGEN AND THE REPEAT RESULT WITH A482 ALLERGEN WERE PROVIDED TO PHYSICIAN(S). THE SAME SAMPLE HAD BEEN TESTED ON (B)(6)2017 ON THE T15 ALLERGEN, RESULTING FALSELY NEGATIVE AND ON THE A482 ALLERGEN, RESULTING POSITIVE. THERE ARE NO KNOWN REPORTS OF PATIENT INTERVENTION DUE TO THE FALSE NEGATIVE T15 ALLERGEN RESULT. THERE ARE NO KNOWN REPORTS OF A DELAY IN ADMINISTERING TREATMENT OR MEDICAL INTERVENTION TO THE PATIENT DUE TO THE FALSE NEGATIVE T15 ALLERGEN RESULT.