MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,06 report with the FDA on 2014-01-17 for IMMULITE 2000 ANDROSTENDIONE L2KA0 manufactured by Siemens Healthcare Diagnostics Inc..
[17389661]
The customer observed high bias on patient samples when using the immulite 2000 androstenedione assay. The customer ran the patient samples on an immulite 2000xpi instrument. The customer stated that the androstenedione results did not match the testosterone results, which were within normal range. There are no known reports of adverse health consequences due to the high bias on patient samples when using the immulite 2000 androstenedione assay.
Patient Sequence No: 1, Text Type: D, B5
[17712104]
Siemens has investigated the incidence of over recovery of patient samples and quality controls on the immulite/immulite1000 androstenedione assay lot number 409 and above, and immulite 2000/immulite 2000 xpi androstenedione assay lot number 314 and above. Siemens has confirmed that these lots are linear up to a concentration of 5. 5 ng/ml, instead of the 10 ng/ml as stated in the instructions for use (ifu). Quality control materials at concentrations between 5. 5 ng/ml and 10 ng/ml will detect this issue. An urgent medical device correction (umdc) 2013-12-19 was sent to us customers and an urgent field safety notice (ufsn) 4008 was sent to ous customers in (b)(6) 2013. The umdc and ufsn state that customers are requested to use quality control materials with at least two levels having concentrations less than 5. 5 ng/ml, and that patient values >5. 5 ng/ml should be verified using an alternate method.
Patient Sequence No: 1, Text Type: N, H10
[33621585]
The original mdr 2432235-2014-00057 was filed on january 17, 2014. Additional information (1/27/14): based on a look back it was noted that this mdr was filed in error as part of the field action for androstenedione, (b)(4). The results reported on androstenedione patient samples were obtained on an alternate platform and not a siemens healthcare instrument or assay.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 2432235-2014-00057 |
| MDR Report Key | 3580162 |
| Report Source | 01,05,06 |
| Date Received | 2014-01-17 |
| Date of Report | 2013-12-18 |
| Date of Event | 2013-05-15 |
| Date Mfgr Received | 2014-01-27 |
| Date Added to Maude | 2014-04-18 |
| 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 | 0 |
| Event Location | 0 |
| Manufacturer Contact | ELIZABETH BEATO |
| Manufacturer Street | 511 BENEDICT AVENUE |
| Manufacturer City | TARRYTOWN NY 10591 |
| Manufacturer Country | US |
| Manufacturer Postal | 10591 |
| Manufacturer Phone | 9145243074 |
| Manufacturer G1 | SIEMENS HEALTHCARE DIAGNOSTICS(REG#3002806944) |
| Manufacturer Street | GLYN RHOWNY LLANBERIS, CAERNARFON |
| Manufacturer City | GWYNEDD, WALES LL54EL |
| Manufacturer Country | UK |
| Manufacturer Postal Code | LL5 4EL |
| Single Use | 3 |
| Remedial Action | RC |
| Previous Use Code | 3 |
| Removal Correction Number | 2432235-01/02/14-001-C |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | IMMULITE 2000 ANDROSTENDIONE |
| Generic Name | IMMULITE 2000 ANDROSTENDIONE |
| Product Code | CIZ |
| Date Received | 2014-01-17 |
| Model Number | IMMULITE 2000 ANDROSTENDIONE |
| Catalog Number | L2KA0 |
| Lot Number | NOT PROVIDED BY CUSTOMER |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | SIEMENS HEALTHCARE DIAGNOSTICS INC. |
| Manufacturer Address | GLYN RHONWY CAERNARFON GWYNEDD, WALES LL554EL UK LL55 4EL |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2014-01-17 |